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A child with intellectual disability and dysmorphism due to complex ring chromosome 6: identification of molecular mechanism with review of literature.
Sheth, Frenny; Liehr, Thomas; Shah, Viraj; Shah, Hillary; Tewari, Stuti; Solanki, Dhaval; Trivedi, Sunil; Sheth, Jayesh.
Afiliação
  • Sheth F; FRIGE's Institute of Human Genetics, FRIGE House, Jodhpur Gam Road, Satellite, Ahmedabad, 380009, India. fshethad1@googlemail.com.
  • Liehr T; University Clinic Jena, Institute of Human Genetics, Am Klinikum 1, 07747, Jena, Germany.
  • Shah V; FRIGE's Institute of Human Genetics, FRIGE House, Jodhpur Gam Road, Satellite, Ahmedabad, 380009, India.
  • Shah H; FRIGE's Institute of Human Genetics, FRIGE House, Jodhpur Gam Road, Satellite, Ahmedabad, 380009, India.
  • Tewari S; FRIGE's Institute of Human Genetics, FRIGE House, Jodhpur Gam Road, Satellite, Ahmedabad, 380009, India.
  • Solanki D; Mantra Child Neurology & Epilepsy Hospital, 3rd floor, Oarnate complex, Kalubha road, Kalanala, Bhavanagar, 364001, India.
  • Trivedi S; FRIGE's Institute of Human Genetics, FRIGE House, Jodhpur Gam Road, Satellite, Ahmedabad, 380009, India.
  • Sheth J; FRIGE's Institute of Human Genetics, FRIGE House, Jodhpur Gam Road, Satellite, Ahmedabad, 380009, India.
Ital J Pediatr ; 44(1): 114, 2018 Oct 11.
Article em En | MEDLINE | ID: mdl-30305128
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Deficiências do Desenvolvimento / Fácies / Transtornos Cromossômicos / Deficiência Intelectual Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Deficiências do Desenvolvimento / Fácies / Transtornos Cromossômicos / Deficiência Intelectual Idioma: En Ano de publicação: 2018 Tipo de documento: Article