Clinical findings and molecular cytogenetic study of de novo pure chromosome 9p deletion: Pre- and postnatal diagnosis
Author:
Funder
National Natural Science Foundation of China
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology
Reference15 articles.
1. Eleven new cases of del(9p) and features from 80 cases;Huret;J Med Genet,1988
2. Clinical and cytogenetic characterization of 13 Dutch patients with deletion 9p syndrome: delineation of the critical region for a consensus phenotype;Swinkels;Am J Med Genet A,2008
3. Detailed characterization of, and clinical correlations in, 10 patients with distal deletions of chromosome 9p;Hauge;Genet Med,2008
4. Narrowing candidate region for monosomy 9p syndrome to a 4.7-Mb segment at 9p22.2-p23;Kawara;Am J Med Genet A,2006
5. Prenatal diagnosis and molecular cytogenetic characterization of a de novo pure distal 9p deletion and literature review;Chen;Genomics,2013
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