sábado, 26 de mayo de 2018

Personal stories or story - OMIM - NCBI

Personal stories or story - OMIM - NCBI

multigenerational African American family

From NIH OMIM

OMIM is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily.



CARDIAC CONDUCTION DEFECT, NONSPECIFIC, INCLUDED
Cytogenetic locations: 3p22.2
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TRUNCATED ACTIN-BINDING PROTEIN, INCLUDED; TABP, INCLUDED
Cytogenetic locations: 3p14.3
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METHYLMALONIC ACIDURIA, mut(0) TYPE, INCLUDED
Cytogenetic locations: 6p12.3
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CHRONIC MOTOR TICS, INCLUDED
Cytogenetic locations: 15q21.2, 1pter-p36.13, 13q31.1
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WT1/EWS FUSION GENE, INCLUDED
Cytogenetic locations: 11p13
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BREAST CANCER, FAMILIAL MALE, INCLUDED
Cytogenetic locations: 2q33.1, 1pter-p36.13, 22q12.1, 1pter-p36.13, 17q23.2, 1pter-p36.13, 17q23.2, 1pter-p36.13, 17q21.33, 1pter-p36.13, 17p13.1, 1pter-p36.13, 16q22.1, 1pter-p36.13, 16p12.2, 1pter-p36.13, 15q15.1, 1pter-p36.13, 14q32.33,2q33.1, 1pter-p36.13, 22q12.1, 1pter-p36.13, 17q23.2, 1pter-p36.13, 17q23.2, 1pter-p36.13, 17q21.33, 1pter-p36.13, 17p13.1, 1pter-p36.13, 16q22.1, 1pter-p36.13, 16p12.2, 1pter-p36.13, 15q15.1, 1pter-p36.13, 14q32.3
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