The breakpoints of the EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) confirmed to 7q11.21 and 9p12 by fluorescence in situ hybridization-Reference-Cited by-同舟云学术

The breakpoints of the EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) confirmed to 7q11.21 and 9p12 by fluorescence in situ hybridization

Published:2008-04-23 Issue:1 Volume:44 Page:50-50
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Fukushima Yoshimitsu,Ohashi Hirofumi,Hasegawa Tomonobu

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1993.tb03843.x/fullpdf

Reference3 articles.

1. Chromosome-band-specific painting: chromosome in situ suppression hybridization using PCR products from a microdissected chromosome band as a probe pool;Deng;Hum Genet,1992

2. EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) with a balanced reciprocal translocation between 7q 11.21 and 9p12 (or 7p11.2 and 9q12) in three generations;Hasegawa;Clin Genet,1991

3. EEC syndrome (ectrodactyly, ectodermal dysplasia and cleft lip/palate) is on 7p11.2-q21.3;Qumsiyeh;Clin Genet,1992

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