Cloning and regional localization of the mouse faciogenital dysplasia (Fgd1) gene.

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作者信息

Pasteris N G, de Gouyon B, Cadle A B, Campbell K, Herman G E, Gorski J L

机构信息

Department of Human Genetics, University of Michigan Medical Center, Ann Arbor 48109-0688, USA.

出版信息

Mamm Genome. 1995 Sep;6(9):658-61. doi: 10.1007/BF00352375.

DOI:10.1007/BF00352375

PMID:8535076

Abstract

摘要

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Aarskog-Scott syndrome: confirmation of linkage to the pericentromeric region of the X chromosome.

Am J Med Genet. 1994 Sep 1;52(3):339-45. doi: 10.1002/ajmg.1320520317.

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Mamm Genome. 1994;5 Spec No:S276-88.

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