Complex chromosome re-arrangement 45,X,t(Y;9) in a girl with sex reversal and mental retardation
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference21 articles.
1. Chromosome Breakage Hotspots and Delineation of the Critical Region for the 9p-Deletion Syndrome
2. Partial duplication of the short arm of chromosome 9 (p13→p22) in a child with typical 9p trisomy phenotype
3. Olfactory Receptor–Gene Clusters, Genomic-Inversion Polymorphisms, and Common Chromosome Rearrangements
4. Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24).
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1. A rare familial rearrangement of chromosomes 9 and 15 associated with intellectual disability: a clinical and molecular study;Molecular Cytogenetics;2021-10-04
2. Early-Onset Gonadoblastoma in a 13-Month-Old Infant with 46,XY Complete Gonadal Dysgenesis Identified with Prenatal Testing: A Case of Chromosome 9P Deletion;AACE Clinical Case Reports;2019-11
3. Unbalanced Y;7 Translocation between Two Low-Similarity Sequences Leading to SRY-Positive 45,X Testicular Disorders of Sex Development;Cytogenetic and Genome Research;2019
4. A rare unbalanced Y:autosome translocation in a Turner syndrome patient;Journal of Pediatric Endocrinology and Metabolism;2018-01-08
5. 9p partial monosomy and disorders of sex development: Review and postulation of a pathogenetic mechanism;American Journal of Medical Genetics Part A;2013-07-03
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