Deletion 9p, duplication 18q in two sisters resulting from a maternal (9;18) (p22;q21.3) translocation
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference28 articles.
1. The 9p- deletion syndrome A patient with a 45,XX,-9,-15, + t(9/15) constitution due to maternal 3:l meiotic disjunction
2. Deletion in the short arm of chromosome 9 from a subject with congenital cerebral maldevelopment
3. (1977): “Clinical Atlas of Human Chromosomes.” New York, Chischester, Brisbane, Toronto: John Wiley & Sons, pp. 87-90.
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Partial trisomy 18q11.2→qter due to de novo unbalanced translocation of chromosomes 15 and 18 analyzed by fluorescence in situ hybridization;Annales de Génétique;2004-10
2. Monosomy 9p24→pter and trisomy 5q31→qter: Case report and review of two cases;American Journal of Medical Genetics;1995-05
3. Confirmation of a cryptic unbalanced translocation using whole chromosome fluorescencein situ hybridization;American Journal of Medical Genetics;1992-11-01
4. Deletion 9p syndrome and malignancy: Acquired vs. constitutional aberrations?;American Journal of Medical Genetics;1992-09-15
5. Partial 18q trisomy and 18p monosomy resulting from a maternal pericentric inversion, inv(18)(p11.2q21.3);Japanese journal of human genetics;1991-09
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