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Spectrum of phenotype and genotype of congenital isolated hypogonadotropic hypogonadism in Asian Indians.
Nair, Sandhya; Jadhav, Swati; Lila, Anurag; Jagtap, Varsha; Bukan, Amol; Pandit, Reshma; Ekbote, Alka; Dharmalingam, Mala; Kumar, Prasanna; Kalra, Pramila; Gandhi, Pramod; Walia, Rama; Sankhe, Shilpa; Raghavan, Vijaya; Shivane, Vyankatesh; Menon, Padma; Bandgar, Tushar; Shah, Nalini.
  • Nair S; Department of Endocrinology, Seth G S Medical College and KEM Hospital, Mumbai, India.
  • Jadhav S; Department of Endocrinology, Seth G S Medical College and KEM Hospital, Mumbai, India.
  • Lila A; Department of Endocrinology, Seth G S Medical College and KEM Hospital, Mumbai, India.
  • Jagtap V; Department of Endocrinology, Seth G S Medical College and KEM Hospital, Mumbai, India.
  • Bukan A; Department of Endocrinology, Seth G S Medical College and KEM Hospital, Mumbai, India.
  • Pandit R; Department of Endocrinology, Seth G S Medical College and KEM Hospital, Mumbai, India.
  • Ekbote A; Kamalnayan Bajaj Hospital, Aurangabad, India.
  • Dharmalingam M; Department of Endocrinology, M.S. Ramaiah Medical College, Bangalore, India.
  • Kumar P; CDEC, Bangalore, India.
  • Kalra P; Department of Endocrinology, M.S. Ramaiah Medical College, Bangalore, India.
  • Gandhi P; Department of Endocrinology, Seth G S Medical College and KEM Hospital, Mumbai, India.
  • Walia R; Department of Endocrinology, P.G.I.M.E.R, Chandigarh, India.
  • Sankhe S; Department of Endocrinology, Seth G S Medical College and KEM Hospital, Mumbai, India.
  • Raghavan V; Department of Endocrinology, Seth G S Medical College and KEM Hospital, Mumbai, India.
  • Shivane V; Department of Endocrinology, Seth G S Medical College and KEM Hospital, Mumbai, India.
  • Menon P; Department of Endocrinology, Seth G S Medical College and KEM Hospital, Mumbai, India.
  • Bandgar T; Department of Endocrinology, Seth G S Medical College and KEM Hospital, Mumbai, India.
  • Shah N; Department of Endocrinology, Seth G S Medical College and KEM Hospital, Mumbai, India.
Clin Endocrinol (Oxf) ; 85(1): 100-9, 2016 07.
Article en En | MEDLINE | ID: mdl-26708526

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fenotipo / Síndrome de Kallmann / Genotipo / Hipogonadismo Tipo de estudio: Clinical_trials / Risk_factors_studies Límite: Female / Humans / Male País como asunto: Asia Idioma: En Año: 2016 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fenotipo / Síndrome de Kallmann / Genotipo / Hipogonadismo Tipo de estudio: Clinical_trials / Risk_factors_studies Límite: Female / Humans / Male País como asunto: Asia Idioma: En Año: 2016 Tipo del documento: Article