Your browser doesn't support javascript.
loading
Gonadal mosaicism of large terminal de novo duplication and deletion in siblings with variable intellectual disability phenotypes.
Rahman, Muhammad M; Uddin, Km Furkan; Al Jezawi, Nesreen K; Karuvantevida, Noushad; Akter, Hosneara; Dity, Nushrat J; Rahaman, Md Ashiquir; Begum, Maksuda; Rahaman, Md Atikur; Baqui, Md Abdul; Salwa, Zeena; Islam, Serajul; Woodbury-Smith, Marc; Basiruzzaman, Mohammed; Uddin, Mohammed.
Afiliação
  • Rahman MM; Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.
  • Uddin KF; NeuroGen Technologies Ltd., Dhaka, Bangladesh.
  • Al Jezawi NK; Holy Family Red Crescent Medical College, Dhaka, Bangladesh.
  • Karuvantevida N; College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.
  • Akter H; College of Medicine, Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates.
  • Dity NJ; Department of Biotechnology, Bharathidasan University, Tiruchirappalli, India.
  • Rahaman MA; NeuroGen Technologies Ltd., Dhaka, Bangladesh.
  • Begum M; NeuroGen Technologies Ltd., Dhaka, Bangladesh.
  • Rahaman MA; NeuroGen Technologies Ltd., Dhaka, Bangladesh.
  • Baqui MA; NeuroGen Technologies Ltd., Dhaka, Bangladesh.
  • Salwa Z; NeuroGen Technologies Ltd., Dhaka, Bangladesh.
  • Islam S; NeuroGen Technologies Ltd., Dhaka, Bangladesh.
  • Woodbury-Smith M; Holy Family Red Crescent Medical College, Dhaka, Bangladesh.
  • Basiruzzaman M; Square Hospital Ltd., Dhaka, Bangladesh.
  • Uddin M; IBN Sina Medical Imaging Center, Dhaka, Bangladesh.
Mol Genet Genomic Med ; 7(10): e00954, 2019 10.
Article em En | MEDLINE | ID: mdl-31475484
Assuntos
Palavras-chave
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Deficiência Intelectual Tipo de estudo: Prognostic_studies Limite: Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Bangladesh
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Deficiência Intelectual Tipo de estudo: Prognostic_studies Limite: Child / Child, preschool / Female / Humans / Male Idioma: En Revista: Mol Genet Genomic Med Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Bangladesh