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Jornal De Pediatria
|
June 15, 2006
Craniovertebral malformation complex in a child with Weismann-Netter-Stuhl syndrome
Ali Al Kaissi, Farid Ben Chehida, Hassan Gharbi, et al.
Skeletal Radiology
|
March 21, 2006
A novel form of ischio-vertebral syndrome
Ali 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 study
Ali Al Kaissi, Sergey Ryabykh, Olga M Pavlova, et al.
Diagnostics (Basel, Switzerland)
|
October 27, 2022
Craniofacial Malformations as Fundamental Diagnostic Tools in Syndromic Entities
Ali Al Kaissi, Sergey Ryabykh, Nabil Nassib, et al.
Medicine
|
September 1, 2017
How frequent is osteogenesis imperfecta in patients with idiopathic osteoporosis?: Case reports
Ali 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 Delays
Christian Windpassinger, Juliette Piard, Carine Bonnard, et al.
Page
of 4
Search research articles
Search
Showing results (31-40 of 36) with videos related to
Sort By:
Page
of 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 syndrome
Ali Al Kaissi, Farid Ben Chehida, Hassan Gharbi, et al.
Skeletal Radiology
|
March 21, 2006
A novel form of ischio-vertebral syndrome
Ali 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 study
Ali Al Kaissi, Sergey Ryabykh, Olga M Pavlova, et al.
Diagnostics (Basel, Switzerland)
|
October 27, 2022
Craniofacial Malformations as Fundamental Diagnostic Tools in Syndromic Entities
Ali Al Kaissi, Sergey Ryabykh, Nabil Nassib, et al.
Medicine
|
September 1, 2017
How frequent is osteogenesis imperfecta in patients with idiopathic osteoporosis?: Case reports
Ali 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 Delays
Christian Windpassinger, Juliette Piard, Carine Bonnard, et al.
Page
of 4