Terminal Deletion of Chromosome 10q and Its Clinical Features
Author:
Publisher
Wiley
Subject
Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1442-200X.1990.tb00788.x/fullpdf
Reference9 articles.
1. Partial deletion 10q
2. Monosomy 10 qter
3. Monosomy 10qter due to a balanced familial translocation: t(10;16)(q25.2;q24)
4. Monosomy 10qter due to a balanced maternal translocation: t(10;8)(q23;p23)
5. Is there a monosomy 10qter syndrome?
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1. Further delineation of EBF3-related syndromic neurodevelopmental disorder in twelve Chinese patients;Frontiers in Pediatrics;2023-03-03
2. Whole Gene Deletion of EBF3 Supporting Haploinsufficiency of This Gene as a Mechanism of Neurodevelopmental Disease;Frontiers in Genetics;2017-10-09
3. 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
4. Monosomy 10q26-qter and trisomy 11q13-qter as a result ofde novo unbalanced translocation;Journal of Applied Genetics;2009-09
5. Urinary retention in a boy with terminal deletion of chromosome 10q at band 26.1;Pediatrics International;2008-08
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