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Mutational analysis of the necdin gene in patients with congenital isolated hypogonadotropic hypogonadism.
Beneduzzi, Daiane; Iyer, Anita K; Trarbach, Ericka Barbosa; Silveira-Neto, Acacio P; Silveira, Letícia G; Tusset, Cintia; Yip, Kathleen; Mendonça, Berenice B; Mellon, Pamela L; Latronico, Ana Claudia.
Affiliation
  • Beneduzzi D; Unidade de Endocrinologia do Desenvolvimento, Laboratório de Hormônios e Genética Molecular/LIM42, Hospital das Clinicas da Faculdade de Medicina da Universidade de São Paulo, Avenida Doutor Eneas de Carvalho Aguiar 155, 2° Andar, Bloco 6, CEP 05403-900 São Paulo, São Paulo, Brazil. daianebeneduzzi@yahoo.com.br
Eur J Endocrinol ; 165(1): 145-50, 2011 Jul.
Article in En | MEDLINE | ID: mdl-21543378
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prader-Willi Syndrome / Hypogonadism Type of study: Prognostic_studies Limits: Animals / Female / Humans / Male Country/Region as subject: America do sul / Brasil Language: En Journal: Eur J Endocrinol Journal subject: ENDOCRINOLOGIA Year: 2011 Document type: Article Affiliation country: Brazil Country of publication: United kingdom
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Prader-Willi Syndrome / Hypogonadism Type of study: Prognostic_studies Limits: Animals / Female / Humans / Male Country/Region as subject: America do sul / Brasil Language: En Journal: Eur J Endocrinol Journal subject: ENDOCRINOLOGIA Year: 2011 Document type: Article Affiliation country: Brazil Country of publication: United kingdom