Further refinement of the candidate region for monosomy 9p syndrome
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.31961/fullpdf
Reference7 articles.
1. Chromosome Breakage Hotspots and Delineation of the Critical Region for the 9p-Deletion Syndrome
2. Diagnostic Genome Profiling in Mental Retardation
3. Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephaly
4. Mutational Screening of FGFR1, CER1, and CDON in a Large Cohort of Trigonocephalic Patients
5. Narrowing candidate region for monosomy 9p syndrome to a 4.7-Mb segment at 9p22.2-p23
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1. Using a new analytic approach for genotyping and phenotyping chromosome 9p deletion syndrome;European Journal of Human Genetics;2024-07-07
2. Insights into the Cardiac Phenotype in 9p Deletion Syndrome: A Multicenter Italian Experience and Literature Review;Genes;2023-01-05
3. From karyotypes to precision genomics in 9p deletion and duplication syndromes;Human Genetics and Genomics Advances;2022-01
4. Postzygotic Breakages of Dicentric Chromosomes: A Rare Mechanism of Terminal Deletions;Cytogenetic and Genome Research;2022
5. Chromosome 9p terminal deletion in nine Egyptian patients and narrowing of the critical region for trigonocephaly;Molecular Genetics & Genomic Medicine;2021-10-05
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