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Citation: Saadi, Irfan et al., Deficiency of the Cytoskeletal Protein SPECC1L Leads to Oblique Facial Clefting, American journal of human genetics (Online) AJHG , 89(1), 2011, pp. 44-55

Authors: Shaheen, Ranad Al-Owain, Mohammed Sakati, Nadia Alzayed, Zayed S. Alkuraya, Fowzan S.

Citation: Shaheen, Ranad et al., FKBP10 and Bruck Syndrome: Phenotypic Heterogeneity or Call for Reclassification?, American journal of human genetics (Online) AJHG , 87(2), 2010, pp. 306-307

Authors: Shaheen, Ranad Faqeih, Eissa Sunker, Asma Morsy, Heba Alkuraya, Fowzan S.

Citation: Shaheen, Ranad et al., Recessive Mutations in DOCK6, Encoding the Guanidine Nucleotide Exchange Factor DOCK6, Lead to Abnormal Actin Cytoskeleton Organization and Adams-Oliver Syndrome, American journal of human genetics (Online) AJHG , 89(2), 2011, pp. 328-333

Authors: Alkuraya, Fowzan S.

Citation: S. Alkuraya, Fowzan, Vogel and Motulsky's Human Genetics, 4th Edition, American journal of human genetics (Online) AJHG , 88(4), 2011, pp. 401-401

Authors: Alkuraya, Fowzan S. Cai, Xuyu Emery, Carina Mochida, Ganeshwaran H. Walsh, Christopher A.

Citation: S. Alkuraya, Fowzan et al., Human Mutations in NDE1 Cause Extreme Microcephaly with Lissencephaly, American journal of human genetics (Online) AJHG , 88(5), 2011, pp. 536-547