Application of fluorescence in situ hybridization for early prenatal diagnosis of partial trisomy 6p/monosomy 6q due to a familial pericentric inversion-Reference-Cited by-同舟云学术

Application of fluorescence in situ hybridization for early prenatal diagnosis of partial trisomy 6p/monosomy 6q due to a familial pericentric inversion

Published:2008-04-23 Issue:5 Volume:44 Page:262-269
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Wauters J. G.,Bossuyt P. J.,Roelen L.,Roy B.,Dumon J.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1993.tb03894.x/fullpdf

Reference35 articles.

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3. Partial trisomy 6p due to familial translocation t(6;20) (p21;p13);Breuning;A new syndrome? Hum Genet,1977

4. Partial 6p trisomy associated with infantile autism;Burd;Clin Genet,1988

5. A 6p trisomy detected in a family with a “giant satellite”;Chiyo;Hum Genet,1975

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3. Pure de novo partial trisomy 6p in a girl with craniosynostosis;American Journal of Medical Genetics Part A;2013-01-10

4. Delineation of Subtelomeric Deletion of the Long Arm of Chromosome 6;Annals of Human Genetics;2011-09-22

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