A. Teebi

A new type of Ehlers‐Danlos syndrome associated with tortuous systemic arteries in a large kindred from Qatar

A. Wahab, IA Janahi, A. Eltohami, 2003, Acta paediatrica.

Absence of PTEN/MMAC1 germ-line mutations in sporadic Bannayan-Riley-Ruvalcaba syndrome.

C. Boland, W. Cavenee, F. Furnari, 1998, Cancer research.

Bone dysplasias: an introduction.

P. Eydoux, F. Fassier, A. Teebi, 1998, Canadian Association of Radiologists journal = Journal l'Association canadienne des radiologistes.

A family exhibiting arterial tortuosity syndrome displays homozygosity for markers in the arterial tortuosity locus at chromosome 20q13

L. Tsui, A. Lindinger, A. Teebi, 2004, Clinical genetics.

Mutation in the cartilage‐derived morphogenetic protein‐1 (CDMP1) gene in a kindred affected with fibular hypoplasia and complex brachydactyly (DuPan syndrome)

L. Tsui, A. Teebi, W. Ahmad, 2002, Clinical genetics.

Bone dysplasia series. Achondroplasia, hypochondroplasia and thanatophoric dysplasia: review and update.

E. Lemyre, P. Glanc, A. Teebi, 1999, Canadian Association of Radiologists journal = Journal l'Association canadienne des radiologistes.

The locus responsible for horizontal gaze palsy/progressive scoliosis and brainstem hypoplasia is refined to a 9‐cM region on chromosome 11q23

L. Tsui, B. Banwell, S. Blaser, 2004, Clinical genetics.

Congenital diaphragmatic abnormalities in arterial tortuosity syndrome patients who carry mutations in the SLC2A10 gene

A. Teebi, I. Peltekova, M. Faiyaz-ul-Haque, 2009, Clinical genetics.

Identification of a p.Ser81Arg encoding mutation in SLC2A10 gene of arterial tortuosity syndrome patients from 10 Qatari families

L. Tsui, A. Teebi, A. Eltohami, 2008, Clinical genetics.