The Bedouin mutation c.155-166del of the TBCE gene in a patient with Sanjad-Sakati syndrome of Moroccan origin-Reference-Cited by-同舟云学术

The Bedouin mutation c.155-166del of the TBCE gene in a patient with Sanjad-Sakati syndrome of Moroccan origin

Published:2015-03 Issue:2 Volume:35 Page:170-172
ISSN:0256-4947
Container-title:Annals of Saudi Medicine
language:en
Short-container-title:Annals of Saudi Medicine

Author:

Ratbi Ilham¹,Lyahyai Jaber¹,Kabiri Meryem²,Banouar Meryem²,Zerkaoui Maria¹³,Barkat Amina²,Sefiani Abdelaziz¹³

Affiliation:

1. Centre de génomique humaine, Faculté de médecine et pharmacie, Université Mohammed, Rabat, Morocco

2. Service de Médecine et Réanimation néonatales, Équipe de Recherche en santé et Nutrition du couple mère enfant, CRECET, Faculté de médecine et pharmacie, Université Mohammed V Souissi, Rabat, Morocco

3. Département de génétique médicale, Institut National d’Hygiène, Rabat, Morocco

Publisher

King Faisal Specialist Hospital and Research Centre

Subject

General Medicine

Reference7 articles.

1. Congenital hypoparathyroidism with dysmorphic features: a new syndrome;Sanjad SA;Pediatr Res,1988

2. A new syndrome of congenital hypoparathyroidism, severe growth failure, and dysmorphic features;Sanjad SA;Arch Dis Child,1991

3. Short stature, mental retardation, and hypoparathyroidism: a new syndrome;Richardson RJ;Arch Dis Child,1990

4. Sanjad Sakati syndrome: a case series from Jordan;Albaramki J;East Mediterr Health J,2012

5. Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42–43;Parvari R;Am J Hum Genet,1998

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