Inherited 15q24 microdeletion syndrome in twins and their father with phenotypic variability
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics,General Medicine
Reference16 articles.
1. Genotype-phenotype correlation in four 15q24 deleted patients identified by array-CGH;Andrieux;Am J Med Genet A,2009
2. 1.5 Mb microdeletion in 15q24 in a patient with mild OAVS phenotype;Brun;Eur J Med Genet,2012
3. Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping;El-Hattab;Hum Genet,2009
4. Deletion and duplication of 15q24: molecular mechanisms and potential modification by additional copy number variants;El-Hattab;Genet Med,2010
5. An additional case of the recurrent 15q24.1 microdeletion syndrome and review of the literature;IS;Twin Res Hum Genet,2011
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1. Prenatal diagnosis of a 15q24.1 microdeletion in a fetus with cerebral and urogenital abnormalities;Clinical Genetics;2024-07-16
2. Hypogammaglobulinemia with T‐cell defects and autoimmune manifestations associated with chromosome 15q24 microdeletion;Scandinavian Journal of Immunology;2023-08-22
3. Reactive oxygen species and their consequences on the structure and function of mammalian spermatozoa;Antioxidants & Redox Signaling;2021-12-16
4. Molecular and phenotypic characteristics of 15q24 microdeletion in pediatric patients with developmental disorders;Molecular Cytogenetics;2021-12
5. Coexistence of urogenital malformations in a female fetus with de novo 15q24 microdeletion and a literature review;Molecular Genetics & Genomic Medicine;2020-05-13
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