From HuGE Literature Finder Database
This database contains published literature on genetic associations and other human genome epidemiology
- High serum serotonin in sudden infant death syndrome.
Proceedings of the National Academy of Sciences of the United States of America 2017 Jul .
Haynes Robin L, Frelinger Andrew L, Giles Emma K, Goldstein Richard D, Tran Hoa, Kozakewich Harry P, Haas Elisabeth A, Gerrits Anja J, Mena Othon J, Trachtenberg Felicia L, Paterson David S, Berry Gerard T, Adeli Khosrow, Kinney Hannah C, Michelson Alan - Candidate gene variants of the immune system and sudden infant death syndrome.
International journal of legal medicine 2016 Mar .
Fard Delnaz, Läer Katharina, Rothämel Thomas, Schürmann Peter, Arnold Matthias, Cohen Marta, Vennemann Mechtild, Pfeiffer Heidi, Bajanowski Thomas, Pfeufer Arne, Dörk Thilo, Klintschar Micha - [High incidence of sudden cardiac death in one family with type-3 long QT syndrome: molecular genetics and electrophysiology mechanism analysis].
Zhonghua xin xue guan bing za zhi 2015 Dec 43 (12): 1046-50.
Zhou Hui, Li Zhang, Ali Raza Ghani, Zhu Wengen, Zhou Qiongqiong, Shen Yang, Xie Jinyan, Cao Qing, Wan Rong, Hu Jinzhu, Hong K - Genetic investigations of sudden unexpected deaths in infancy using next-generation sequencing of 100 genes associated with cardiac diseases.
European journal of human genetics : EJHG 2015 Sep .
Hertz Christin Loeth, Christiansen Sofie Lindgren, Larsen Maiken Kudahl, Dahl Morten, Ferrero-Miliani Laura, Weeke Peter Ejvind, Pedersen Oluf, Hansen Torben, Grarup Niels, Ottesen Gyda Lolk, Frank-Hansen Rune, Banner Jytte, Morling Nie - That's not it, either-neither polymorphisms in PHOX2B nor in MIF are involved in sudden infant death syndrome (SIDS).
International journal of legal medicine 2015 Sep 129 (5): 985-9.
Poetsch Micaela, Todt Rebecca, Vennemann Mechtild, Bajanowski Thom
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