What can we learn from old microdeletion syndromes using array-CGH screening?-Reference-Cited by-同舟云学术

What can we learn from old microdeletion syndromes using array-CGH screening?

Published:2011-07-26 Issue:1 Volume:82 Page:41-47
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Mosca-Boidron A L,Bouquillon S,Faivre L,Callier P,Andrieux J,Marle N,Bonnet C,Vincent-Delorme C,Berri M,Plessis G,Manouvrier-Hanu S,Dieux-Coeslier A,Thauvin-Robinet C,Pipiras E,Delahaye A,Payet M,Ragon C,Masurel-Paulet A,Questiaux E,Benzacken B,Jonveaux P,Mugneret F,Holder-Espinasse M

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2011.01747.x/fullpdf

Reference25 articles.

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3. The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome.;Shaffer;Genet Med,2007

4. Delineation of 15q13.3 microdeletions.;Masurel-Paulet;Clin Genet,2010

5. Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals.;Bijlsma;Eur J Med Genet,2009

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