الرئيسية › دليل الباحثين › Cherif Beldjord

Cherif Beldjord

الانتماء : Université Paris Descartes

• 8منشورات (انتماء فرنسي)
• 181مجموع المنشورات
• 11111الاستشهادات
• 46مؤشر h

OpenAlex

مجالات البحث

• Genetics and Neurodevelopmental Disorders
• Genomics and Rare Diseases
• Fetal and Pediatric Neurological Disorders
• Hemoglobinopathies and Related Disorders
• Cystic Fibrosis Research Advances

المنشورات (8)

• Mosaic parental germline mutations causing recurrent forms of malformations of cortical development
  2015 · European Journal of Human Genetics · استُشهد به 41 مرة
• Exploration moléculaire des lissencéphalies : à propos de quatre cas
  2014 · Revue Neurologique
• Molecular Heterogeneity of β-Thalassemia in Algeria: How to Face Up to a Major Health Problem
  2009 · Hemoglobin · استُشهد به 21 مرة
• A new gene involved in X-linked mental retardation identified by analysis of an X;2 balanced translocation
  2000 · Nature Genetics · استُشهد به 239 مرة
• Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity
  1995 · Nature Genetics · استُشهد به 188 مرة
• The spectrum of β‐thalassaemia in Algeria: possible origins of the molecular heterogeneity and a tentative diagnostic strategy
  1993 · British Journal of Haematology · استُشهد به 22 مرة
• A novelβthalassemia gene with a single base mutation in the conserved polypyrimidine sequence at the 3′ end of IVS 2
  1988 · Nucleic Acids Research · استُشهد به 33 مرة
• DNA haplotype distribution in Algerian ? thalassaemia patients
  1988 · Human Genetics · استُشهد به 20 مرة

المؤلفون المشاركون

• Dominique Labie
• Alain Carrié
• Claudine Lapouméroulie
• Jamel Chelly
• Nathalie Carion
• Kaplan Jc
• Bettina Bessières
• Axel Kahn
• Josée Pagnier
• Marie Claude Vinet
• Nicole Philip
• Michel Fardeau

البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).