Unbalanced 18q/21q translocation in a patient previously reported as monosomy 21

Author:

Riegel M.,Hargreaves P.,Baumer A.,Guc-Scekic M.,Ignjatovic M.,Schinzel A.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference38 articles.

1. A case of 21 monosomy;Garzicic;Ann. Genet. (Paris),1988

2. Catalogue of Unbalanced Chromosome Aberrations in Man, second ed;Schinzel,2001

3. De novo unbalanced t(11q;21q) leading to a partial monosomy 21pter-q22.2 and 11q24-qter in a patient initially diagnosed as monosomy 21;Riegel;Genet. Couns.,2001

4. Full monosomy 21, prenatally diagnosed by fluorescent in situ hybridisation;Joosten;Prenat. Diagn.,1996

5. Proximal deletion of chromosome 21 confirmed by in situ hybridization and molecular studies;Courtens;Am. J. Med. Genet.,1994

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