HLBS-PopOmics - Heart, Lung, Blood, and Sleep Disorders Knowledge Base in Population Genomics - CDC-Authored Genomics Publication Database|Home|PHGKB

CDC-Authored Genomics Publication Database|Home|PHGKB

HLBS-PopOmics

- Heart, Lung, Blood, and Sleep Disorders Knowledge Base in Population Genomics -

Publication
Prevalence of Asthma, Asthma Attacks, and Emergency Department Visits for Asthma Among Working Adults - National Health Interview Survey, 2011-2016.   Mazurek Jacek M et al. MMWR. Morbidity and mortality weekly report 2018 Apr 67(13) 377-386
Prevalence and Predictors of Cholesterol Screening, Awareness, and Statin Treatment Among US Adults With Familial Hypercholesterolemia or Other Forms of Severe Dyslipidemia (1999-2014).   Bucholz Emily M et al. Circulation 2018 Mar
Current Cigarette Smoking Among Adults - United States, 2016.   Jamal Ahmed et al. MMWR. Morbidity and mortality weekly report 2018 Jan 67(2) 53-59
Time to treatment for rifampicin-resistant tuberculosis: systematic review and meta-analysis.   Boyd R et al. The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease 2017 Nov 21(11) 1173-1180
Rhinovirus Viremia in Patients Hospitalized with Community Acquired Pneumonia.   Lu Xiaoyan et al. The Journal of infectious diseases 2017 Aug
Human Bocavirus Capsid Messenger RNA Detection in Children With Pneumonia.   Schlaberg Robert et al. The Journal of infectious diseases 2017 Sep 216(6) 688-696
Estimating global, regional and national rotavirus deaths in children aged <5 years: Current approaches, new analyses and proposed improvements.   Clark Andrew et al. PloS one 2017 12(9) e0183392
Cascade Screening for Familial Hypercholesterolemia and the Use of Genetic Testing.   Knowles Joshua W et al. JAMA 2017 318(4) 381-382
Greater Cognitive Deficits with Sleep-Disordered Breathing among Individuals with Genetic Susceptibility to Alzheimer's Disease: The Multi-Ethnic Study of Atherosclerosis.   Johnson Dayna A et al. Annals of the American Thoracic Society 2017 Jul
Genome-wide association study to identify variants associated with vaso-occlusive pain in sickle cell anemia.   Chaturvedi Shruti et al. Blood 2017 Jun
Evaluation of Pneumococcal Load in Blood by Polymerase Chain Reaction for the Diagnosis of Pneumococcal Pneumonia in Young Children in the PERCH Study.   Deloria Knoll Maria et al. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2017 Jun (suppl_3) S357-S367
Is Higher Viral Load in the Upper Respiratory Tract Associated With Severe Pneumonia? Findings From the PERCH Study.   Feikin Daniel R et al. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2017 Jun (suppl_3) S337-S346
Detection of Pneumococcal DNA in Blood by Polymerase Chain Reaction for Diagnosing Pneumococcal Pneumonia in Young Children From Low- and Middle-Income Countries.   Morpeth Susan C et al. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2017 Jun (suppl_3) S347-S356
The Enduring Challenge of Determining Pneumonia Etiology in Children: Considerations for Future Research Priorities.   Feikin Daniel R et al. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2017 Jun 64(suppl_3) S188-S196
Colonization Density of the Upper Respiratory Tract as a Predictor of Pneumonia-Haemophilus influenzae, Moraxella catarrhalis, Staphylococcus aureus, and Pneumocystis jirovecii.   Park Daniel E et al. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2017 Jun (suppl_3) S328-S336
Density of Upper Respiratory Colonization With Streptococcus pneumoniae and Its Role in the Diagnosis of Pneumococcal Pneumonia Among Children Aged <5 Years in the PERCH Study.   Baggett Henry C et al. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2017 Jun 64(suppl_3) S317-S327
Limited Utility of Polymerase Chain Reaction in Induced Sputum Specimens for Determining the Causes of Childhood Pneumonia in Resource-Poor Settings: Findings From the Pneumonia Etiology Research for Child Health (PERCH) Study.   Thea Donald M et al. Clinical infectious diseases : an official publication of the Infectious Diseases Society of America 2017 Jun (suppl_3) S289-S300
Clinical and bacteriological characteristics associated with clustering of multidrug-resistant tuberculosis.   J-Y Feng J-Y et al. The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease 2017 May
Influence of Antibiotics on the Detection of Bacteria by Culture-Based and Culture-Independent Diagnostic Tests in Patients Hospitalized With Community-Acquired Pneumonia.   Harris Aaron M et al. Open forum infectious diseases 2017 (1) ofx014
Viral Pathogen Detection by Metagenomics and Pan Viral Group PCR in Children with Pneumonia Lacking Identifiable Etiology.   Schlaberg Robert et al. The Journal of infectious diseases 2017 Mar
Subtypes and risk behaviors among incident HIV cases in the Bangkok Men Who Have Sex with Men Cohort Study, Thailand, 2006-2015.   Lam Caitlin R et al. AIDS research and human retroviruses 2016 Dec
Emergency department utilization by Californians with sickle cell disease, 2005-2014.   Paulukonis Susan T et al. Pediatric blood & cancer 2017 Jun 64(6)
Serology Enhances Molecular Diagnosis of Respiratory Virus Infections Other than Influenza in Children and Adults Hospitalized with Community-Acquired Pneumonia.   Zhang Yange et al. Journal of clinical microbiology 2016 Oct
Association of sputum microbiota profiles with severity of community-acquired pneumonia in children.   Pettigrew Melinda M et al. BMC infectious diseases (1) 317
The use of whole genome sequencing for detecting antimicrobial resistance in nontyphoidal Salmonella.   McDermott Patrick F et al. Antimicrobial agents and chemotherapy 2016 Jul
Genome Structural Diversity among 31 Bordetella pertussis Isolates from Two Recent U.S. Whooping Cough Statewide Epidemics.   Bowden Katherine E et al. mSphere 1(3)
Cardiac Tropism of Borrelia burgdorferi: An Autopsy Study of Sudden Cardiac Death Associated with Lyme Carditis.   Muehlenbachs Atis et al. The American journal of pathology 2016 Mar
Achievements, challenges and unmet needs for haemophilia patients with inhibitors: Report from a symposium in Paris, France on 20 November 2014.  Dargaud Y et al. Haemophilia : the official journal of the World Federation of Hemophilia 2016 Jan 22 Suppl 11-24
Whole Genome Sequencing Analysis Accurately Predicts Antimicrobial Resistance Phenotypes in Campylobacter.   Zhao S et al. Applied and environmental microbiology 2015 Oct
SHATTUCK LECTURE: The Future of Public Health.   Frieden Thomas R et al. The New England journal of medicine 2015 Oct (18) 1748-54
Molecular Detection and Characterization of Mycoplasma pneumoniae Among Patients Hospitalized With Community-Acquired Pneumonia in the United States.   Diaz Maureen H et al. Open forum infectious diseases 2015 Sep (3) ofv106
Game, set, match for factor VIII mismatch?   Miller Connie H et al. Blood 2015 Aug 13. 126(7) 829-30
Bartonella spp. and Coxiella burnetii Associated with Community-Acquired, Culture-Negative Endocarditis, Brazil.   Siciliano Rinaldo Focaccia et al. Emerging Infect. Dis. 2015 Aug (8) 1429-32
Detection of critical congenital heart defects: Review of contributions from prenatal and newborn screening.   Olney Richard S et al. Semin. Perinatol. 2015 Apr 39(3) 230-7
A statistical approach for rare-variant association testing in affected sibships.   Epstein Michael P et al. Am. J. Hum. Genet. 2015 Apr 2. 96(4) 543-54
Evaluation of von Willebrand factor phenotypes and genotypes in Hemophilia A patients with and without identified F8 mutations.   Boylan B et al. J. Thromb. Haemost. 2015 Jun 13(6) 1036-42
Evolution of the "drivers" of translational cancer epidemiology: analysis of funded grants and the literature.   Lam Tram Kim et al. Am. J. Epidemiol. 2015 Apr 1. 181(7) 451-8
Genetic variants in TNFa, TGFB1, PTGS1 and PTGS2 genes are associated with diisocyanate-induced asthma.   Yucesoy Berran et al. J Immunotoxicol 2015 Feb 27. 1-8
Improving newborn screening for cystic fibrosis using next-generation sequencing technology: a technical feasibility study.   Baker Mei W et al. Genet. Med. 2015 Feb 12.
Prevalence of and trends in dyslipidemia and blood pressure among US children and adolescents, 1999-2012.   Kit Brian K et al. JAMA Pediatr 2015 Mar 169(3) 272-9
Incidence of sickle cell trait--United States, 2010.   Ojodu Jelili et al. MMWR Morb. Mortal. Wkly. Rep. 2014 Dec 12. 63(49) 1155-8
Reducing the burden of disease and death from familial hypercholesterolemia: a call to action.   Knowles Joshua W et al. Am. Heart J. 2014 Dec 168(6) 807-11
Universal state newborn screening programs can reduce health disparities.   Brosco Jeffrey P et al. JAMA Pediatr 2015 Jan 169(1) 7-8
The Cancer Genomics and Epidemiology Navigator: An NCI online tool to enhance cancer epidemiology research.   Schully Sheri D et al. Cancer Epidemiol. Biomarkers Prev. 2014 Nov 23(11) 2610-1
Health policy for sickle cell disease in Africa: experience from Tanzania on interventions to reduce under-five mortality.   Makani Julie et al. Trop. Med. Int. Health 2015 Feb 20(2) 184-7
Investigations of Mycoplasma pneumoniae infections in the United States: trends in molecular typing and macrolide resistance from 2006 to 2013.   Diaz Maureen H et al. J. Clin. Microbiol. 2015 Jan 53(1) 124-30
An overview of recommendations and translational milestones for genomic tests in cancer.   Chang Christine Q et al. Genet. Med. 2015 Jun 17(6) 431-40
Mortality of New York children with sickle cell disease identified through newborn screening.   Wang Ying et al. Genet. Med. 2015 Jun 17(6) 452-9
The next generation of large-scale epidemiologic research: implications for training cancer epidemiologists.   Spitz Margaret R et al. Am. J. Epidemiol. 2014 Nov 15. 180(10) 964-7
Understanding and improving health education among first-time parents of infants with sickle cell anemia in Alabama: a mixed methods approach.   Lebensburger Jeffrey D et al. J. Pediatr. Hematol. Oncol. 2015 Jan 37(1) 35-42
Vaccine-associated varicella and rubella infections in severe combined immunodeficiency with isolated CD4 lymphocytopenia and mutations in IL7R detected by tandem whole exome sequencing and chromosomal microarray.   Bayer D K et al. Clin. Exp. Immunol. 2014 Dec 178(3) 459-69
Severity of rhinovirus infection in hospitalized adults is unrelated to genotype.   McCulloch Denise J et al. Am. J. Clin. Pathol. 2014 Aug 142(2) 165-72
Association between alcohol and cardiovascular disease: Mendelian randomisation analysis based on individual participant data.   Holmes Michael V et al. BMJ 2014 349g4164
State-based surveillance for selected hemoglobinopathies.   Hulihan Mary M et al. Genet. Med. 2015 Feb 17(2) 125-30
Actionable diagnosis of neuroleptospirosis by next-generation sequencing.   Wilson Michael R et al. N. Engl. J. Med. 2014 Jun 19. 370(25) 2408-17
Donor-derived West Nile virus infection in solid organ transplant recipients: report of four additional cases and review of clinical, diagnostic, and therapeutic features.   Winston Drew J et al. Transplantation 2014 May 15. 97(9) 881-9
Genetic variants in the major histocompatibility complex class I and class II genes are associated with diisocyanate-induced Asthma.   Yucesoy Berran et al. J. Occup. Environ. Med. 2014 Apr 56(4) 382-7
Determination of accuracy of polycythemia vera diagnoses and use of the JAK2V617F test in the diagnostic scheme.   Roda Paul et al. Ann. Hematol. 2014 Sep 93(9) 1467-72
Discordance between self-report and genetic confirmation of sickle cell disease status in African-American adults.   Bean Christopher J et al. Public Health Genomics 2014 17(3) 169-72
Maternal smoking, xenobiotic metabolizing enzyme gene variants, and gastroschisis risk.   Jenkins Mary M et al. Am. J. Med. Genet. A 2014 Jun 164A(6) 1454-63
Prothrombin G20210A mutation is associated with young-onset stroke: the genetics of early-onset stroke study and meta-analysis.   Jiang Baijia et al. Stroke 2014 Apr 45(4) 961-7
The CDC Hemophilia B mutation project mutation list: a new online resource.   Li Tengguo et al. Mol Genet Genomic Med 2013 Nov 1(4) 238-45
Prioritizing genomic applications for action by level of evidence: a horizon-scanning method.   Dotson W D et al. Clinical pharmacology and therapeutics 2014 Apr 95(4) 394-402
A public health economic assessment of hospitals' cost to screen newborns for critical congenital heart disease.   Peterson Cora et al. Public Health Rep 129(1) 86-93
Mutation analysis of a cohort of US patients with hemophilia B.   Li Tengguo et al. Am. J. Hematol. 2014 Apr 89(4) 375-9
Availability of an assay for detecting Mycobacterium tuberculosis, including rifampin-resistant strains, and considerations for its use - United States, 2013.   et al. MMWR Morb. Mortal. Wkly. Rep. 2013 Oct 18. 62(41) 821-7
Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia.   Bean Christopher J et al. Br. J. Haematol. 2013 Oct 163(2) 268-76
The geometric increase in meta-analyses from China in the genomic era.   Ioannidis John P A et al. PLoS ONE 2013 8(6) e65602
The microRNA-200 family targets multiple non-small cell lung cancer prognostic markers in H1299 cells and BEAS-2B cells.   Pacurari Maricica et al. Int. J. Oncol. 2013 Aug 43(2) 548-60
The use of US health insurance data for surveillance of rare disorders: hereditary hemorrhagic telangiectasia.   Grosse Scott D et al. Genet. Med. 2014 Jan 16(1) 33-9
Comparative effectiveness research in cancer genomics and precision medicine: current landscape and future prospects.   Simonds Naoko I et al. J. Natl. Cancer Inst. 2013 Jul 3. 105(13) 929-36
Prioritizing tuberculosis clusters by genotype for public health action, Washington, USA.   Lindquist Scott et al. Emerging Infect. Dis. 2013 Mar 19(3) 493-6
Association of the Period3 clock gene length polymorphism with salivary cortisol secretion among police officers.   Wirth Michael et al. Neuro Endocrinol. Lett. 2013 34(1) 27-37
Telomere length and elevated iron: the influence of phenotype and HFE genotype.   Mainous Arch G et al. Am. J. Hematol. 2013 Jun 88(6) 492-6
Transforming epidemiology for 21st century medicine and public health.   Khoury Muin J et al. Cancer Epidemiol. Biomarkers Prev. 2013 Apr 22(4) 508-16
Utilization of epidermal growth factor receptor (EGFR) testing in the United States: a case study of T3 translational research.   Lynch Julie A et al. Genet. Med. 2013 Aug 15(8) 630-8
Relationships between selected gene polymorphisms and blood pressure sensitivity to weight loss in elderly persons with hypertension.   Kostis William J et al. Hypertension 2013 Apr 61(4) 857-63
Provocative questions in cancer epidemiology in a time of scientific innovation and budgetary constraints.   Lam Tram Kim et al. Cancer Epidemiol. Biomarkers Prev. 2013 Apr 22(4) 496-500
"Drivers" of translational cancer epidemiology in the 21st century: needs and opportunities.   Lam Tram Kim et al. Cancer Epidemiol. Biomarkers Prev. 2013 Feb 22(2) 181-8
The CDC Hemophilia A Mutation Project (CHAMP) mutation list: a new online resource.   Payne Amanda B et al. Hum. Mutat. 2013 Feb 34(2) E2382-91
Narcolepsy as an adverse event following immunization: case definition and guidelines for data collection, analysis and presentation.   Poli Francesca et al. Vaccine 2013 Jan 30. 31(6) 994-1007
Newborn screening for critical congenital heart disease: essential public health roles for birth defects monitoring programs.   Olney Richard S et al. Birth Defects Res. Part A Clin. Mol. Teratol. 2012 Dec 94(12) 965-9
Knowledge integration in cancer: current landscape and future prospects.   Ioannidis John P A et al. Cancer Epidemiol. Biomarkers Prev. 2013 Jan 22(1) 3-10
Genotypic characterization of Streptococcus infantarius subsp. coli isolates from sea otters with infective endocarditis and/or septicemia and from environmental mussel samples.   Counihan-Edgar Katrina L et al. J. Clin. Microbiol. 2012 Dec 50(12) 4131-3
Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease.  Bean Christopher J et al. Blood 2012 Nov 1. 120(18) 3822-8
Multiwalled carbon nanotube-induced gene signatures in the mouse lung: potential predictive value for human lung cancer risk and prognosis.   Guo Nancy L et al. J. Toxicol. Environ. Health Part A 2012 75(18) 1129-53
Survival among people with Down syndrome: a nationwide population-based study in Denmark.   Zhu Jin Liang et al. Genet. Med. 2013 Jan 15(1) 64-9
A smoking-associated 7-gene signature for lung cancer diagnosis and prognosis.   Wan Ying-Wooi et al. Int. J. Oncol. 2012 Oct 41(4) 1387-96
Utility of multiplex ligation-dependent probe amplification (MLPA) for hemophilia mutation screening.   Payne A B et al. J. Thromb. Haemost. 2012 Sep 10(9) 1951-4
Family history of myocardial infarction is a risk factor for venous thromboembolism among whites but not among blacks.   Mili Fatima D et al. Clin. Appl. Thromb. Hemost. 19(4) 410-7
Genetic variants in antioxidant genes are associated with diisocyanate-induced asthma.   Yucesoy Berran et al. Toxicol. Sci. 2012 Sep 129(1) 166-73
The Jamaican historical experience of the impact of educational interventions on sickle cell disease child mortality.   Grosse Scott D et al. Am J Prev Med 2012 Jun 42(6) e101-3
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.   Milton Jacqueline N et al. PLoS ONE 2012 7(4) e34741
Chronic occupational exposure to arsenic induces carcinogenic gene signaling networks and neoplastic transformation in human lung epithelial cells.   Stueckle Todd A et al. Toxicol. Appl. Pharmacol. 2012 Jun 1. 261(2) 204-16
Experiences from the Shiga toxin-producing Escherichia coli O104:H4 outbreak in Germany and research needs in the field, Berlin, 28-29 November 2011.   et al. Euro Surveill. 2012 17(7)
Pneumococcal genome sequencing tracks a vaccine escape variant formed through a multi-fragment recombination event.   Golubchik Tanya et al. Nat. Genet. 2012 Mar 44(3) 352-5
F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis.   Gouw Samantha C et al. Blood 2012 Mar 22. 119(12) 2922-34
CFTR mutation analysis and haplotype associations in CF patients.   Cordovado S K et al. Mol. Genet. Metab. 2012 Feb 105(2) 249-54
F8 and F9 mutations in US haemophilia patients: correlation with history of inhibitor and race/ethnicity.   Miller C H et al. Haemophilia 2012 May 18(3) 375-82
Public health implications of sickle cell trait: a report of the CDC meeting.   Grant Althea M et al. Am J Prev Med 2011 Dec 41(6 Suppl 4) S435-9
Screening U.S. college athletes for their sickle cell disease carrier status.   Jordan Lanetta B et al. Am J Prev Med 2011 Dec 41(6 Suppl 4) S406-12
Sickle cell disease in Africa: a neglected cause of early childhood mortality.   Grosse Scott D et al. Am J Prev Med 2011 Dec 41(6 Suppl 4) S398-405
Sickle cell disease: the need for a public health agenda.   Yusuf Hussain R et al. Am J Prev Med 2011 Dec 41(6 Suppl 4) S376-83
A public health framework for rare blood disorders.   Grosse Scott D et al. Am J Prev Med 2011 Dec 41(6 Suppl 4) S319-23
Serology as an adjunct to polymerase chain reaction assays for surveillance of acute respiratory virus infections.   Sawatwong Pongpun et al. Clin. Infect. Dis. 2012 Feb 1. 54(3) 445-6
The ACE I/D polymorphism in US adults: limited evidence of association with hypertension-related traits and sex-specific effects by race/ethnicity.   Ned Renée M et al. Am. J. Hypertens. 2012 Feb 25(2) 209-15
Lack of maternal folic acid supplementation is associated with heart defects in Down syndrome: a report from the National Down Syndrome Project.   Bean Lora J H et al. Birth Defects Res. Part A Clin. Mol. Teratol. 2011 Oct 91(10) 885-93
The association of variants in the FTO gene with longitudinal body mass index profiles in non-Hispanic white children and adolescents.   Hallman D M et al. Int J Obes (Lond) 2012 Jan 36(1) 61-8
Accuracy of self-reported family history is strongly influenced by the accuracy of self-reported personal health status of relatives.   Janssens A Cecile J W et al. J Clin Epidemiol 2012 Jan 65(1) 82-9
Cost-effectiveness analysis of diagnostic options for pneumocystis pneumonia (PCP).   Harris Julie R et al. PLoS ONE 2011 6(8) e23158
Genetic associations with metabolic syndrome and its quantitative traits by race/ethnicity in the United States.   Vassy Jason L et al. Metab Syndr Relat Disord 2011 Dec 9(6) 475-82
IRon Overload screeNing tool (IRON): development of a tool to guide screening in primary care.   Mainous Arch G et al. Am. J. Hematol. 2011 Sep 86(9) 733-7
Ethical implications and practical considerations of ethnically targeted screening for genetic disorders: the case of hemoglobinopathy screening.   Hinton Cynthia F et al. Ethn Health 16(4-5) 377-88
The contribution of chromosomal abnormalities to congenital heart defects: a population-based study.   Hartman Robert J et al. Pediatr Cardiol 2011 Dec 32(8) 1147-57
Investigation of a researcher's death due to septicemic plague.   Frank Karen M et al. N. Engl. J. Med. 2011 Jun 30. 364(26) 2563-4
Birth prevalence rates of newborn screening disorders in relation to screening practices in the United States.   Hertzberg Vicki S et al. J. Pediatr. 2011 Oct 159(4) 555-60
Multi-walled carbon nanotube-induced gene expression in the mouse lung: association with lung pathology.   Pacurari M et al. Toxicol. Appl. Pharmacol. 2011 Aug 15. 255(1) 18-31
Varenicline for smoking cessation: nausea severity and variation in nicotinic receptor genes.   Swan G E et al. Pharmacogenomics J. 2012 Aug 12(4) 349-58
Blood gene expression profiling detects silica exposure and toxicity.   Sellamuthu Rajendran et al. Toxicol. Sci. 2011 Aug 122(2) 253-64
Screening for sudden cardiac death in the young: report from a national heart, lung, and blood institute working group.   Kaltman Jonathan R et al. Circulation 2011 May 3. 123(17) 1911-8
Implementation of the first worldwide quality assurance program for cystic fibrosis multiple mutation detection in population-based screening.   Earley Marie C et al. Clin. Chim. Acta 2011 Jul 15. 412(15-16) 1376-81
Inhalation exposure of gas-metal arc stainless steel welding fume increased atherosclerotic lesions in apolipoprotein E knockout mice.   Erdely Aaron et al. Toxicol. Lett. 2011 Jul 4. 204(1) 12-6
Feasibility, diagnostic accuracy, and effectiveness of decentralised use of the Xpert MTB/RIF test for diagnosis of tuberculosis and multidrug resistance: a multicentre implementation study.   Boehme Catharina C et al. Lancet 2011 Apr 30. 377(9776) 1495-505
Hexamethylene diisocyanate asthma is associated with genetic polymorphisms of CD14, IL-13, and IL-4 receptor a.   Bernstein David I et al. J. Allergy Clin. Immunol. 2011 Aug 128(2) 418-20
Newborn screening for cystic fibrosis: a paradigm for public health genetics policy development. Proceedings of a 1997 workshop.   et al. MMWR. Recommendations and reports : Morbidity and mortality weekly report. Recommendations and reports 1997 Dec 46(RR-16) 1-24