Your browser doesn't support javascript.
loading
Clinical and Molecular Characterization of Prader-Willi Syndrome.
Sanjeeva, G N; Maganthi, Madhuri; Kodishala, Himabindu; Marol, Rohit Kumar R; Kulshreshtha, Pooja S; Lorenzetto, Elisa; Kadandale, Jayarama S; Hladnik, Uros; Raghupathy, P; Bhat, Meenakshi.
Afiliação
  • Sanjeeva GN; Department of Pediatric Genetics, Indira Gandhi Institute of Child Health, South Hospital Complex, Dharmaram College Post, Bangalore, Karnataka, 560 029, India. sanju_gn@rediffmail.com.
  • Maganthi M; Department of Pediatric Genetics, Indira Gandhi Institute of Child Health, South Hospital Complex, Dharmaram College Post, Bangalore, Karnataka, 560 029, India.
  • Kodishala H; Department of Pediatric and Adolescent Endocrinology, Indira Gandhi Institute of Child Health, Bangalore, Karnataka, India.
  • Marol RKR; Department of Pediatric Genetics, Indira Gandhi Institute of Child Health, South Hospital Complex, Dharmaram College Post, Bangalore, Karnataka, 560 029, India.
  • Kulshreshtha PS; Department of Molecular Cytogeneticis, Centre for Human Genetics, Bangalore, Karnataka, India.
  • Lorenzetto E; "Mauro Baschirotto" Institute for Rare Diseases, B.I.R.D. Foundation, Vicenza, Italy.
  • Kadandale JS; Department of Molecular Cytogeneticis, Centre for Human Genetics, Bangalore, Karnataka, India.
  • Hladnik U; "Mauro Baschirotto" Institute for Rare Diseases, B.I.R.D. Foundation, Vicenza, Italy.
  • Raghupathy P; Department of Pediatric and Adolescent Endocrinology, Indira Gandhi Institute of Child Health, Bangalore, Karnataka, India.
  • Bhat M; Department of Pediatric Genetics, Indira Gandhi Institute of Child Health, South Hospital Complex, Dharmaram College Post, Bangalore, Karnataka, 560 029, India.
Indian J Pediatr ; 84(11): 815-821, 2017 Nov.
Article em En | MEDLINE | ID: mdl-28660389
Assuntos
Palavras-chave
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Prader-Willi Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Indian J Pediatr Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Índia
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Prader-Willi Tipo de estudo: Diagnostic_studies / Screening_studies Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Indian J Pediatr Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Índia