Terminal deletion of 6p results in a recognizable phenotype
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference22 articles.
1. Cryptic subtelomeric 6p deletion in a girl with congenital malformations and severe language impairment
2. Mild developmental delay in terminal chromosome 6p deletion
3. Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the region
4. Delineation of two distinct 6p deletion syndromes
5. Phenotypic and molecular assessment of seven patients with 6p25 deletion syndrome: Relevance to ocular dysgenesis and hearing impairment
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3. Novel maternal duplication of 6p22.3-p25.3 with subtelomeric 6p25.3 deletion: new clinical findings and genotype–phenotype correlations;Molecular Cytogenetics;2023-06-11
4. The phenotypic spectrum of terminal and subterminal 6p deletions based on a social media-derived cohort and literature review;Orphanet Journal of Rare Diseases;2023-03-24
5. Chromosome 6p25 deletion syndrome: A case report and review of ophthalmic features;American Journal of Medical Genetics Part A;2023-03-20
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