De novo small supernumerary marker chromosomes detected on 143 000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches-Reference-Cited by-同舟云学术

De novo small supernumerary marker chromosomes detected on 143 000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches

Published:2014-02-11 Issue:5 Volume:34 Page:460-468
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat Diagn

Author:

Malvestiti Francesca¹,De Toffol Simona¹,Grimi Beatrice¹,Chinetti Sara¹,Marcato Livia¹,Agrati Cristina¹,Di Meco Anna Maria¹,Frascoli Giuditta¹,Trotta Anna¹,Malvestiti Barbara¹,Ruggeri Anna¹,Dulcetti Francesca¹,Maggi Federico¹,Simoni Giuseppe¹,Grati Francesca Romana¹

Affiliation:

1. Research and Development, Cytogenetics and Molecular Biology; TOMA Advanced Biomedical Assays; Busto Arsizio Varese Italy

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pd.4330/fullpdf

Reference26 articles.

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2. Small supernumerary marker chromosomes (sSMC) in humans;Liehr;Cytogenet Genome Res,2004

3. Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics;Liehr;Int J Mol Med,2007

4. Supernumerary marker chromosomes in man: parental origin, mosaicism and maternal age revisited;Crolla;Eur J Hum Genet,2005

5. Cytogenetic and molecular evaluation of 241 small supernumerary marker chromosomes: cooperative study of 19 Italian laboratories;Dalpra;Genet Med,2005

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