Congenital duplication of the palm syndromeAL-QATTAN, M. M; EYAID, Wafaa; AL-BALWI, Mohammed et al.Annals of plastic surgery. 2007, Vol 59, Num 3, pp 341-343, issn 0148-7043, 3 p.Article

A Novel Homozygous Missense Mutation (c.610G>A, p.Gly204Ser) in the WNT7A Gene Causes Tetra-amelia in Two Saudi FamiliesEYAID, Wafaa; AL-QATTAN, Mohammad M; AL ABDULKAREEM, Ibrahim et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 3, pp 599-604, issn 1552-4825, 6 p.Article

A Novel Mutation in the SHH Long-Range Regulator (ZRS) Is Associated With Preaxial Polydactyly, Triphalangeal Thumb, and Severe Radial Ray DeficiencyAL-QATTAN, Mohammad M; AL ABDULKAREEM, Ibrahim; AL HAIDAN, Yazied et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 10, pp 2610-2615, issn 1552-4825, 6 p.Article

Transaldolase deficiency: report of 12 new cases and further delineation of the phenotypeEYAID, Wafaa; AL HARBI, Talal; ANAZI, Shamsa et al.Journal of inherited metabolic disease. 2013, Vol 36, Num 6, pp 997-1004, issn 0141-8955, 8 p.Article

The genetic basis of a craniofacial disease provides insight into COPII coat assemblyFROMME, J. Christopher; RAVAZZOLA, Mariella; HAMAMOTO, Susan et al.Developmental cell. 2007, Vol 13, Num 5, pp 623-636, issn 1534-5807, 14 p.Article

Novel point mutations and mutational complexes in the enhancer II, core promoter and precore regions of hepatitis B virus genotype D1 associated with hepatocellular carcinoma in Saudi ArabiaKHAN, Anis; AL BALWI, Mohammed A; MIZOKAMI, Masashi et al.International journal of cancer (Print). 2013, Vol 133, Num 12, pp 2864-2871, issn 0020-7136, 8 p.Article