Evidence that FGFR1 loss-of-function mutations may cause variable skeletal malformations in patients with Kallmann syndrome

标题
Evidence that FGFR1 loss-of-function mutations may cause variable skeletal malformations in patients with Kallmann syndrome
作者
关键词
-
出版物
Advances in Medical Sciences
Volume 57, Issue 2, Pages 314-321
出版商
Elsevier BV
发表日期
2013-01-18
DOI
10.2478/v10039-012-0036-4

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