Duplication of the distal segment of 14q
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference24 articles.
1. Familial translocation involving chromosome 6, 14 and 20, identified by quinacrine fluorescence
2. A child trisomic for the distal part of chromosome 14q.
3. Genes for immunoglobulin heavy chains and for α1-antitrypsin are localized to specific regions of chromosome 14q
4. Partial trisomy 14q due to familial t(14q-, 11q+) translocation
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1. A Recurrent De Novo Terminal Duplication of 14q32 in Korean Siblings Associated with Developmental Delay and Intellectual Disability, Growth Retardation, Facial Dysmorphism, and Cerebral Infarction: A Case Report and Literature Review;Genes;2021-09-07
2. Rearrangement of Chromosome 14q with Associated White Matter Disease;Pediatric Neurology;2011-08
3. A de novo 7.6Mb tandem duplication of 14q32.2-qter associated with primordial short stature with neurosecretory growth hormone dysfunction, distinct facial anomalies and mild developmental delay;European Journal of Medical Genetics;2008-07
4. Unbalanced karyotype, dup 14(q13-q22), in a mother and her two children;Clinical Genetics;2008-06-28
5. Familial translocation t(10;14) (q26.1;q32.3): report of three offspring with 10q deletion and 14q duplication;Clinical Genetics;2008-06-28
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