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A Novel Homozygous Missense Mutation in the Zinc Finger DNA Binding Domain of GLI1 Causes Recessive Post-Axial Polydactyly.
Umair, Muhammad; Ahmad, Farooq; Ahmad, Saeed; Alam, Qamre; Rehan, Mohd; Alqosaibi, Amany I; Alnamshan, Mashael M; Rafeeq, Misbahuddin M; Haque, Shahnaz; Sain, Ziaullah M; Ismail, Muhammad; Alfadhel, Majid.
Afiliação
  • Umair M; Medical Genomics Research Department, King Abdullah International Medical Research Center (KAIMRC), King Saud bin Abdulaziz University for Health Science, Ministry of National Guard-Health Affairs (MNGHA), Riyadh, Saudi Arabia.
  • Ahmad F; Department of Chemistry, Women University Swabi, Swabi, Pakistan.
  • Ahmad S; Consultant Orthopedic Surgeon, Capital Hospital Islamabad, Islamabad, Pakistan.
  • Alam Q; Medical Genomics Research Department, King Abdullah International Medical Research Center (KAIMRC), King Saud bin Abdulaziz University for Health Science, Ministry of National Guard-Health Affairs (MNGHA), Riyadh, Saudi Arabia.
  • Rehan M; King Fahd Medical Research Center, King Abdulaziz University, Jeddah, Saudi Arabia.
  • Alqosaibi AI; Department of Medical Laboratory Technology, Faculty of Applied Medical Sciences, King Abdulaziz University, Jeddah, Saudi Arabia.
  • Alnamshan MM; Department of Biology, College of Science, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.
  • Rafeeq MM; Department of Biology, College of Science, Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia.
  • Haque S; Department of Pharmacology, Faculty of Medicine, Rabigh, King Abduaziz University, Jeddah, Saudi Arabia.
  • Sain ZM; Department of Pharmacology, Faculty of Medicine, Rabigh, King Abduaziz University, Jeddah, Saudi Arabia.
  • Ismail M; Department of Microbiology, Faculty of Medicine, Rabigh, King Abduaziz University, Jeddah, Saudi Arabia.
  • Alfadhel M; Department of Chemistry, Women University Swabi, Swabi, Pakistan.
Front Genet ; 12: 746949, 2021.
Article em En | MEDLINE | ID: mdl-34721536
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies Idioma: En Revista: Front Genet Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Arábia Saudita País de publicação: Suíça
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Prognostic_studies Idioma: En Revista: Front Genet Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Arábia Saudita País de publicação: Suíça