Normal intelligence and premature ovarian failure in an adult female with a 7.6 Mb de novo terminal deletion of chromosome 9p
Author:
Funder
Wellcome Trust
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference29 articles.
1. Deletion of the short arm of chromosome no. 9 (46,9p-): a new deletion syndrome;Alfi;Ann. Genet.,1973
2. Narrowing candidate region for monosomy 9p syndrome to a 4.7-Mb segment at 9p22.2–p23;Kawara;Am. J. Med. Genet. A,2006
3. Chromosome breakage hotspots and delineation of the critical region for the 9p-deletion syndrome;Christ;Am. J. Hum. Genet.,1999
4. 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
5. Chromosome 9p deletion syndrome and sex reversal: novel findings and redefinition of the critically deleted regions;Onesimo;Am. J. Med. Genet. A,2012
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