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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Nov 29, 2023. (Total: 223447Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Sudden Infant Death and PHOX2B[original query]
Sudden infant death syndrome: case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development.
Pediatric research 2004 Sep 56 (3): 391-5.
Weese-Mayer Debra E, Berry-Kravis Elizabeth M, Zhou Lili, Maher Brion S, Curran Mark E, Silvestri Jean M, Marazita Mary
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
Non-polyalanine repeat mutation in PHOX2B is detected in autopsy cases of sudden unexpected infant death.
PloS one 2022 4 17 (4): e0267751.
Ueda Atsushi, Osawa Motoki, Naito Haruaki, Ochiai Eriko, Kakimoto
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