Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies-Reference-Cited by-同舟云学术

Forty-two supernumerary marker chromosomes (SMCs) in 43 273 prenatal samples: chromosomal distribution, clinical findings, and UPD studies

Published:2005-08-03 Issue:11 Volume:13 Page:1192-1204
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Bartsch Oliver,Loitzsch Anne,Kozlowski Peter,Mazauric Marie-Luise,Hickmann Gabriele

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/5201473.pdf

Reference36 articles.

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3. Warburton D : De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints. Am J Hum Genet 1991; 49: 995–1013.

4. Blennow E, Bui TH, Kristoffersson U et al: Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: prevalence and characterization by fluorescence in situ hybridization. Prenat Diagn 1994; 11: 1019–1028.

5. Brondum-Nielsen K, Mikkelsen M : A 10-year survey, 1980–1990, of prenatally diagnosed small supernumerary marker chromosomes, identified by FISH analysis. Outcome and follow-up of 14 cases diagnosed in a series of 12 699 prenatal samples. Prenat Diagn 1995; 15: 615–619.

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