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在“
Wiley电子期刊
”中,
命中:
1
条,耗时:小于0.01 秒
1.
Application of whole-exome sequencing to unravel the molecular basis of undiagnosed syndromic congenital neutropenia with intellectual disability
作者:
Alexandra Gauthier-Vasserot
;
Christel Thauvin-Robinet
;
Ange-Line Bruel
;
Yannis Duffourd
;
Judith St-Onge
;
Thibaud Jouan
;
Jean-Baptiste Riviè
;
re
;
Delphine Heron
;
Jean Donadieu
;
Christine Bellanné
;
-
Chantelot
;
Claire Briandet
;
Fré
;
dé
;
ric Huet
;
Paul Kuentz
;
Daphné
;
Lehalle
;
Laurence Duplomb-Jego
;
Elodie Gautier
;
Isabelle Maystadt
;
Lucile Pinson
;
Daniel Amram
;
Salima El Chehadeh
;
Judith Melki
;
Sophia Julia
;
Laurence Faivre and Julien Thevenon
刊名:American Journal of Medical Genetics Part A
出版年:2017
1
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2017年(1)
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