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African Health Sciences|October 26, 2005
Subtotal amelia in a child with autosomal recessive hypohidrotic ectodermal dysplasiaAli Al Kaissi, Farid Ben Chehida, Nabil Nassib, et al.Genes|October 27, 2022
Combining Gene Mutation with Expression of Candidate Genes to Improve Diagnosis of Escobar SyndromeDorra Najjar, Asma Chikhaoui, Sinda Zarrouk, et al.Spine|May 25, 2006
Progressive congenital torticollis in VATER association syndromeAli Al Kaissi, Farid Ben Chehida, Hatem Safi, et al.Diagnostics (Basel, Switzerland)|July 27, 2022
Torticollis in Connection with Spine PhenotypeAli Al Kaissi, Nabil Nassib, Sami Bouchoucha, et al.Diagnostics (Basel, Switzerland)|October 27, 2022
Craniofacial Malformations as Fundamental Diagnostic Tools in Syndromic EntitiesAli Al Kaissi, Sergey Ryabykh, Nabil Nassib, et al.Pageof 1