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期刊论文FSCN1 as a Candidate Gene for Syndromic Intellectual Disability? Evidence From a Recurrent Variant in an Iranian Cohort复制

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出版社: Wiley
作者: Hossein Najmabadi; Tara Akhtarkhavari; Ebrahim Shokouhian; Sanaz Arzhangi; Kimia Kahrizi

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