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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Hyperplasia and CFTR[original query]
[Prevalence of frequent recessive diseases in the Spanish population through DNA analyses on samples from the neonatal screening].
Medicina clínica 2005 Oct 125 (13): 493-5.
Ezquieta Begoña, Ruano Miguel L F, Dulín Elena, Arnao Dolores R, Rodríguez Ampa
Variation in MSRA modifies risk of neonatal intestinal obstruction in cystic fibrosis.
PLoS genetics 2012 8 (3): e1002580.
Henderson Lindsay B, Doshi Vishal K, Blackman Scott M, Naughton Kathleen M, Pace Rhonda G, Moskovitz Jackob, Knowles Michael R, Durie Peter R, Drumm Mitchell L, Cutting Garry
PRSS1_p.Leu81Met mutation results in autoimmune pancreatitis.
World journal of gastroenterology : WJG 2013 Jun 19 (21): 21.
Gao F, Li YM, Hong GL, Xu ZF, Liu QC, He QL, Lin LQ, Weng SH
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