Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactyly

Please use this identifier to cite or link to this item: http://140.112.115.32:8080/ir/handle/987654321/1390

Title:	Phenotypic features of pure 9p deletion in a male infant include cryptorchidism, congenital heart defects and postaxial polydactyly
Authors:	Chih-Ping Chen;Shuan-Pei Lin;Ming-Ren Chen;Jun-Wei Su;Schu-Rern Chern;Yen-Jiun Chen;Meng-Shan Lee;Wayseen Wang
Contributors:	生醫所
Date:	2012-06-01
Issue Date:	2015-03-16 15:43:31 (UTC+8)
Relation:	Genetic Counseling 23，195-200
Appears in Collections:	[Institute of Biomedical Sciences] Journal papers

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