Ring 21 chromosome: the mild end of the phenotypic spectrum
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1986.tb01912.x/fullpdf
Reference14 articles.
1. Acute lymphoblastic leukemia in two children with a congenital chromosome anomaly: Familial inv(11) (p15q13) in one and ring chromosome No. 21 in the other;Cabrol;Cancer Genet. Cytogenet.,1983
2. The chromosomal basis of human infertility;Chandley;Br. Med. Bull.,1979
3. The cytogenetic and clinical implications of a ring chromosome 2;Cote;Ann. Genet. (Paris).,1981
4. Down's syndrome with a recombinant tandem duplication of chromosome 21 derived from a maternal ring;Howell;J. Med. Genet.,1984
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1. Transmission of ring chromosome 13 from a mother to daughter with both having a 46,XX, r(13)(p13q34) karyotype;American Journal of Medical Genetics;2004
2. Chromosomal Anomalies and the Eye;Pediatric Ophthalmology and Strabismus;2003
3. Cytogenetic and molecular analysis of a ring (21) in a patient with partial trisomy 21 and megakaryocytic leukemia;American Journal of Medical Genetics;1995-07
4. Prenatal diagnosis of familial ring 21 chromosome;Prenatal Diagnosis;1995-03
5. Chromosomal Anomalies and the Eye;Handbook of Pediatric Eye and Systemic Disease
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