受强制性开放获取政策约束的文章 - Habiba Chaabouni-Bouhamed了解详情
可在其他位置公开访问的文章：4 篇
Diagnostic exome sequencing to elucidate the genetic basis of likely recessive disorders in consanguineous families
P Makrythanasis, M Nelis, FA Santoni, M Guipponi, A Vannier, F Béna, ...
Human mutation 35 (10), 1203-1210, 2014
强制性开放获取政策： Swiss National Science Foundation, European Commission
Molecular analysis of Bardet-Biedl syndrome families: report of 21 novel mutations in 10 genes
J Chen, N Smaoui, MBH Hammer, X Jiao, SA Riazuddin, S Harper, ...
Investigative ophthalmology & visual science 52 (8), 5317-5324, 2011
强制性开放获取政策： US National Institutes of Health
Conference report: Second conference of the Middle East and North Africa newborn screening initiative: Partnerships for sustainable newborn screening infrastructure and …
JWHRRHMNBSSC Danuta Krotoski, Sorrel Namaste, Randa Kamal Raouf, Ibrahim El ...
Genetics IN Medicine 11 (9), 663-68, 2009
强制性开放获取政策： US National Institutes of Health, National Institute of Health and Medical …
RE (ACT) 2014 Rare Diseases. 2nd International Congress on Research of Rare and Orphan Diseases. 5th to 8th March 2014, Gehry Building, Novartis Campus, Basel: Abstracts
BD Solomon, F Hadziselimovic, NO Hadziselimovic, P Demougin, ...
Molecular Syndromology 5 (2), 87-99, 2014
强制性开放获取政策： Government of Spain
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