Rare interstitial deletion 9q31.2 to q33.1 de novo: Longitudinal study in a patient over a period of more than 20 years
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
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1. Further characterization of the 9q31 microdeletion phenotype; delineation of a common region of overlap containing ZNF462;Molecular Genetics & Genomic Medicine;2022-12-03
2. Overlapping Interstitial Deletions of the Region 9q22.33 to 9q33.3 of Three Patients Allow Pinpointing Candidate Genes for Epilepsy and Cleft Lip and Palate;Molecular Syndromology;2022-10-27
3. A novel familial 9q31.2q32 microdeletion: Muscle cramping, somnolence, fatigue, sensorineural hearing loss, pubertal delay, and short stature;Clinical Case Reports;2019-01-07
4. Delineation of the 9q31 deletion syndrome: Genomic microarray characterization of two patients with overlapping deletions;American Journal of Medical Genetics Part A;2018-10-22
5. Krüppel-like factor 4 expression in oral carcinoma cells and hypermethylation at the gene promoter;BMC Oral Health;2016-02-04
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