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Farid Ben Chehida

Showing results (31-40 of 36) with videos related to

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Jornal De Pediatria|June 15, 2006
Craniovertebral malformation complex in a child with Weismann-Netter-Stuhl syndromeAli Al Kaissi, Farid Ben Chehida, Hassan Gharbi, et al.
Skeletal Radiology|March 21, 2006
A novel form of ischio-vertebral syndromeAli Al Kaissi, Ali Al Kassi, Farid Ben Chehida, et al.
Medicine|January 5, 2019
The Managment of cervical spine abnormalities in children with spondyloepiphyseal dysplasia congenita: Observational studyAli Al Kaissi, Sergey Ryabykh, Olga M Pavlova, 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.
Medicine|September 1, 2017
How frequent is osteogenesis imperfecta in patients with idiopathic osteoporosis?: Case reportsAli Al Kaissi, Christian Windpassinger, Farid Ben Chehida, et al.
American Journal of Human Genetics|September 9, 2017
CDK10 Mutations in Humans and Mice Cause Severe Growth Retardation, Spine Malformations, and Developmental DelaysChristian Windpassinger, Juliette Piard, Carine Bonnard, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Jornal De Pediatria|June 15, 2006
Craniovertebral malformation complex in a child with Weismann-Netter-Stuhl syndromeAli Al Kaissi, Farid Ben Chehida, Hassan Gharbi, et al.
Skeletal Radiology|March 21, 2006
A novel form of ischio-vertebral syndromeAli Al Kaissi, Ali Al Kassi, Farid Ben Chehida, et al.
Medicine|January 5, 2019
The Managment of cervical spine abnormalities in children with spondyloepiphyseal dysplasia congenita: Observational studyAli Al Kaissi, Sergey Ryabykh, Olga M Pavlova, 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.
Medicine|September 1, 2017
How frequent is osteogenesis imperfecta in patients with idiopathic osteoporosis?: Case reportsAli Al Kaissi, Christian Windpassinger, Farid Ben Chehida, et al.
American Journal of Human Genetics|September 9, 2017
CDK10 Mutations in Humans and Mice Cause Severe Growth Retardation, Spine Malformations, and Developmental DelaysChristian Windpassinger, Juliette Piard, Carine Bonnard, et al.
Pageof 4