Deletion (14) (q24.3q32.1): Evidence for a distinct clinical phenotype
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference11 articles.
1. Deletion of band 13q21 is compatible with normal phenotype
2. Genes for immunoglobulin heavy chains and for α1-antitrypsin are localized to specific regions of chromosome 14q
3. A child with multiple congenital anomalies and karyotype 46,XY,del(14)(q31q32.3): Further delineation of chromosome 14 interstitial deletion syndrome
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1. A 14q31.1-q32.11 deletion case: Genotype – Neurological Phenotype Correlations in 14q interstitial deletion syndrome;Romanian Biotechnological Letters;2020-06-06
2. Dental anomalies in craniofacial microsomia: A systematic review;Orthodontics & Craniofacial Research;2019-10-28
3. FoxN3 is necessary for the development of the interatrial septum, the ventricular trabeculae and the muscles at the head/trunk interface in the African clawed frog, Xenopus laevis (Lissamphibia: Anura: Pipidae);Developmental Dynamics;2019-03-28
4. Interstitial 14q24.3 to q31.3 deletion in a 6-year-old boy with a non-specific dysmorphic phenotype;Molecular Cytogenetics;2014-11-19
5. Dental findings in 14q terminal deletion syndrome;Clinical Dysmorphology;2014-04
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