Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: Syndrome and GSS[original query] |
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Epistatic interactions with a common hypomorphic RET allele in syndromic Hirschsprung disease. Human mutation 2007 Aug 28 (8): 790-6. de Pontual L, Pelet A, Clement-Ziza M, Trochet D, Antonarakis S E, Attie-Bitach T, Beales P L, Blouin J-L, Dastot-Le Moal F, Dollfus H, Goossens M, Katsanis N, Touraine R, Feingold J, Munnich A, Lyonnet S, Amiel |
Early detection of abnormal prion protein in genetic human prion diseases now possible using real-time QUIC assay. PloS one 2013 8 (1): 1. Sano K, Satoh K, Atarashi R, Takashima H, Iwasaki Y, Yoshida M, Sanjo N, Murai H, Mizusawa H, Schmitz M, Zerr I, Kim YS, Nishida N |
Malignant testicular germ cell tumors in postpubertal individuals with androgen insensitivity: prevalence, pathology and relevance of single nucleotide polymorphism-based susceptibility profiling. Human reproduction (Oxford, England) 2017 11 32 (12): 2561-2573. Cools M, Wolffenbuttel K P, Hersmus R, Mendonca B B, Kaprová J, Drop S L S, Stoop H, Gillis A J M, Oosterhuis J W, Costa E M F, Domenice S, Nishi M Y, Wunsch L, Quigley C A, T'Sjoen G, Looijenga L H |
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- Page last updated:Apr 16, 2024
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