Cargando…
Clinical Features of Aberrations Chromosome 22q: A Pilot Study
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 the 22q chromosome, are now well-defined. Ou...
Autores principales: | Atli, Emine Ikbal, Atli, Engin, Yalcintepe, Sinem, Demir, Selma, Mail, Cisem, Eker, Damla, Ozen, Yasemin, Gurkan, Hakan |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Georg Thieme Verlag KG
2021
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8837404/ https://www.ncbi.nlm.nih.gov/pubmed/35169783 http://dx.doi.org/10.1055/s-0041-1739496 |
Ejemplares similares
-
The Frequency of
SMN1, SMN2
Copy Numbers in 246 Turkish Cases Analyzed with MLPA Method
por: Yalcintepe, Sinem, et al.
Publicado: (2023) -
Investigation the Relationship of Autism Spectrum Disorder and FOXP2, GRIN2B, KATNAL2, GABRA4 Genes
por: YALÇINTEPE, Sinem, et al.
Publicado: (2021) -
Investigation of Genetic Alterations in Congenital Heart Diseases in Prenatal Period
por: Atli, Emine Ikbal, et al.
Publicado: (2021) -
The Importance of Targeted Next-Generation Sequencing Usage in Cytogenetically Normal Myeloid Malignancies
por: Atli, Emine Ikbal, et al.
Publicado: (2021) -
Comprehensive Genetic Analysis Results of TSC1/TSC2 Genes in Patients with Clinical Suspicion of Tuberous Sclerosis Complex and Definition of 3 Novel Variants
por: Demir, Selma, et al.
Publicado: (2021)