Case Reports
doi: 10.1111/j.1399-0004.1977.tb01303.x.
The 9p- deletion syndrome. A patient with a 45, XX-9, -15, +t(9/15) constitution due to maternal 3:1 meiotic disjunction
- PMID: 837573
- DOI: 10.1111/j.1399-0004.1977.tb01303.x
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Case Reports
The 9p- deletion syndrome. A patient with a 45, XX-9, -15, +t(9/15) constitution due to maternal 3:1 meiotic disjunction
Clin Genet.
1977 Mar.
Abstract
Deletion of the short arm of chromosome 9, derived from a 3:1 meiotic segregation in the mother, carrier of a balanced 9/15 translocation, was found in a 3-year-old female. Severe psychomotor retardation with delayed speech, brachicephaly, flat occiput hypertelorism and long upper lip were the main signs in the girl.
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