受强制性开放获取政策约束的文章 - Capucine Hyon了解详情
无法在其他位置公开访问的文章：1 篇
Expanding the clinical and neuroradiologic phenotype of primary microcephaly due to ASPM mutations
S Passemard, L Titomanlio, M Elmaleh, A Afenjar, JL Alessandri, G Andria, ...
Neurology 73 (12), 962-969, 2009
强制性开放获取政策： National Institute of Health and Medical Research, France
可在其他位置公开访问的文章：4 篇
Loss of function of the nuclear receptor NR2F2, encoding COUP-TF2, causes testis development and cardiac defects in 46, XX children
A Bashamboo, C Eozenou, A Jorgensen, J Bignon-Topalovic, JP Siffroi, ...
The American Journal of Human Genetics 102 (3), 487-493, 2018
强制性开放获取政策： National Institute for Health Research, UK, Wellcome Trust, European Commission
Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies
MF Portnoi, MC Dumargne, S Rojo, SF Witchel, AJ Duncan, C Eozenou, ...
Human molecular genetics 27 (7), 1228-1240, 2018
强制性开放获取政策： US National Institutes of Health, 中国科学院, 国家自然科学基金委员会, UK …
Deletion of CPEB1 Gene: A Rare but Recurrent Cause of Premature Ovarian Insufficiency
C Hyon, L Mansour-Hendili, S Chantot-Bastaraud, B Donadille, V Kerlan, ...
The Journal of Clinical Endocrinology & Metabolism 101 (5), 2099-2104, 2016
强制性开放获取政策： National Institute of Health and Medical Research, France
Genomic and clinical characteristics of six patients with partially overlapping interstitial deletions at 10p12p11
C Wentzel, E Rajcan-Separovic, CAL Ruivenkamp, S Chantot-Bastaraud, ...
European journal of human genetics 19 (9), 959-964, 2011
强制性开放获取政策： Canadian Institutes of Health Research
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