Mild developmental delay in terminal chromosome 6p deletion
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference18 articles.
1. Partial Deletion of Chromosome 6p: Autopsy Findings in a Premature Infant and Review of the Literature
2. Cryptic subtelomeric 6p deletion in a girl with congenital malformations and severe language impairment
3. Ring chromosome 6: Report of a patient and literature review
4. Evidence of a locus for orofacial clefting on human chromosome 6p24 and STS content map of the region
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1. A case of childhood glaucoma with a combined partial monosomy 6p25 and partial trisomy 18p11 due to an unbalanced translocation;Ophthalmic Genetics;2020-03-03
2. Prenatal diagnosis of 6pter-p24 deletion syndrome in a fetus from a Han Chinese family;Medicine;2020-02
3. Cerebral White Matter Lesions and Dysmorphisms: Signs Suggestive of 6p25 Deletion Syndrome—Literature Review;Journal of Pediatric Genetics;2019-08-04
4. Phenotype of a Belgian Family With 6p25 Deletion Syndrome;Annals of Otology, Rhinology & Laryngology;2016-07-20
5. Dilated Virchow-Robin spaces mimicking white matter disease in a XYY syndrome;Journal of Pediatric Neurology;2015-07-30
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