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Two heterozygous mutations of the AMH gene in a Japanese patient with persistent Müllerian duct syndrome.
Morikawa, Shuntaro; Moriya, Kimihiko; Ishizu, Katsura; Tajima, Toshihiro.
J Pediatr Endocrinol Metab ; 27(11-12): 1223-6, 2014 Nov.
Article in En | MEDLINE | ID: mdl-25026127
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cryptorchidism / Anti-Mullerian Hormone / Disorder of Sex Development, 46,XY / Heterozygote / Mutation Type of study: Prognostic_studies Limits: Humans / Infant / Male Language: En Journal: J Pediatr Endocrinol Metab Journal subject: ENDOCRINOLOGIA / PEDIATRIA Year: 2014 Document type: Article Country of publication: Germany
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cryptorchidism / Anti-Mullerian Hormone / Disorder of Sex Development, 46,XY / Heterozygote / Mutation Type of study: Prognostic_studies Limits: Humans / Infant / Male Language: En Journal: J Pediatr Endocrinol Metab Journal subject: ENDOCRINOLOGIA / PEDIATRIA Year: 2014 Document type: Article Country of publication: Germany