Interstitial deletion of chromosome 21
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1982.tb01436.x/fullpdf
Reference28 articles.
1. Partial trisomy and monosomy 21 in an infant with an unusual de novo 21/21 translocation;Cantu;Ann. Génét.,1980
2. Evidence for a correlation between late replication and autosomal gene inactivation in a familial translocation t(X;21);Couturier;Hum. Genet.,1979
3. Identification of 21r and 22r chromosomes by quinacrine fluorescence;Crandall;Clin. Genet.,1972
4. Normal phenotype and partial trisomy for the G positive region of chromosome 21;Daniel;J. med. Genet.,1979
5. De novo simultaneous reciprocal translocation and deletion;Fried;J. med. Genet.,1978
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1. De novo balanced 5;21 translocation in a child with acrobrachycephaly, ventriculomegaly, pulmonary stenosis, ectopic anus and mental retardation;Clinical Genetics;2008-06-28
2. Monosomy 21q: two cases of del(21q) and review of the literature;Clinical Genetics;2008-06-28
3. A familial interstitial deletion of the long arm of chromosome 21;Clinical Genetics;2008-06-28
4. Pure proximal deletion of chromosome 21 and kyphosis;European Journal of Medical Genetics;2007-11
5. Familial transmission of a deletion of chromosome 21 derived from a translocation between chromosome 21 and an inverted chromosome 22;American Journal of Medical Genetics;1997-06-27
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