Clinical Features of Aberrations Chromosome 22q: A Pilot Study

Autor: Emine Ikbal Atli, Engin Atli, Sinem Yalcintepe, Selma Demir, Cisem Mail, Damla Eker, Yasemin Ozen, Hakan Gurkan

Publikováno v: Global Medical Genetics, Vol 09, Iss 01, Pp 042-050 (2022)

Objective A significant number of genetic variations have been identified in chromosome 22, using molecular genetic techniques. Various genomic disorders on chromosome 22, including cat's eye syndrome caused by extra copies of the proximal region of

Externí odkaz: https://doaj.org/article/2234d8b3151a4c60a88032b94d8a5b4a

Clinical Features of Aberrations Chromosome 22q: A Pilot Study.

Autor: Atli EI; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Atli E; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Yalcintepe S; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Demir S; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Mail C; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Eker D; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Ozen Y; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey., Gurkan H; Department of Medical Genetics, Faculty of Medicine, Trakya University, Edirne, Turkey.

Publikováno v: Global medical genetics [Glob Med Genet] 2021 Nov 09; Vol. 9 (1), pp. 42-50. Date of Electronic Publication: 2021 Nov 09 (Print Publication: 2022).