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Surgical Neurology|January 24, 2006
Type I congenital multiple intraspinal extradural cysts associated with distichiasis and lymphedema syndromeImad N Kanaan, Nadia Sakati, Faisal OtaibiAnnals of Saudi Medicine|December 3, 2004
Cytogenetics and etiology of ambiguous genitalia in 120 pediatric patientsAngham Al-Mutair, M Anwar Iqbal, Nadia Sakati, et al.Asian Journal of Surgery|August 1, 2006
Persistent hyperinsulinaemic hypoglycaemia of infancy in 43 children: long-term clinical and surgical follow-upSaleh Al-Nassar, Nadia Sakati, Abdullah Al-Ashwal, et al.American Journal of Medical Genetics. Part A|August 1, 2007
Four siblings with distal renal tubular acidosis and nephrocalcinosis, neurobehavioral impairment, short stature, and distinctive facial appearance: a possible new autosomal recessive syndromeEissa Faqeih, Samhar I Al-Akash, Nadia Sakati, et al.Community Genetics|March 16, 2005
Recently available techniques applicable to genetic problems in the Middle EastPinar T Ozand, Ali Al Odaib, Nadia Sakati, et al.Molecular Human Reproduction|October 7, 2004
Multiple displacement amplification on single cell and possible PGD applicationsAli Hellani, Serdar Coskun, Moncef Benkhalifa, et al.Saudi Medical Journal|April 9, 2002
Long-term follow up of carbonic anhydrase II deficiency syndromeMohammad Awad, Abdullah A Al-Ashwal, Nadia Sakati, et al.Genes|December 15, 2020
Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing LossKhushnooda Ramzan, Nouf S Al-Numair, Sarah Al-Ageel, et al.Journal of Pediatric Surgery|March 25, 2008
Pheochromocytoma in children and adolescents: a clinical spectrumNabil K Bissada, Ahmed S Safwat, Raouf M Seyam, et al.Endocrine Connections|June 17, 2021
25-Hydroxylase vitamin D deficiency in 27 Saudi Arabian subjects: a clinical and molecular report on CYP2R1 mutationsSarah Bakhamis, Faiqa Imtiaz, Khushnooda Ramzan, et al.Pageof 2