Terminal deletion of chromosome 10q at band 26.1: Follow-up in an adolescent male with high-output renal failure from congenital obstructive uropathy
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference14 articles.
1. Terminal deletion of chromosome 10q26 due to a paternal translocation {(7;10)(q36;q26)}
2. Severe mental retardation in six generations of a large South African family carrying a translocation t(6;10)(q27;q25.2).
3. A further case of monosomy 10qter
4. Terminal deletion of the long arm of chromosome 10: Case report and review of the literature
5. Terminal Deletion of Chromosome 10q and Its Clinical Features
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1. Early Intervention for Renal Dysfunction due to Terminal Deletion of Chromosome 10q by Monitoring Cystatin-C;Journal of Nihon University Medical Association;2022-06-01
2. Whole Gene Deletion of EBF3 Supporting Haploinsufficiency of This Gene as a Mechanism of Neurodevelopmental Disease;Frontiers in Genetics;2017-10-09
3. Genetic Aspects of Congenital Urologic Anomalies;European Urology Supplements;2015-04
4. Chromosome 10q Deletion del (10)(q26.1q26.3) is Associated with Cataract;Pediatrics & Neonatology;2013-04
5. Complex distal 10q rearrangement in a girl with mild intellectual disability: Follow up of the patient and review of the literature of non-acrocentric satellited chromosomes;American Journal of Medical Genetics Part A;2011-09-30
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