Refinement of a 400-kb Critical Region Allows Genotypic Differentiation between Isolated Lissencephaly, Miller-Dieker Syndrome, and Other Phenotypes Secondary to Deletions of 17p13.3-Reference-Cited by-同舟云学术

Refinement of a 400-kb Critical Region Allows Genotypic Differentiation between Isolated Lissencephaly, Miller-Dieker Syndrome, and Other Phenotypes Secondary to Deletions of 17p13.3

Published:2003-04 Issue:4 Volume:72 Page:918-930
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Cardoso Carlos,Leventer Richard J.,Ward Heather L.,Toyo-oka Kazuhito,Chung June,Gross Alyssa,Martin Christa L.,Allanson Judith,Pilz Daniela T.,Olney Ann H.,Mutchinick Osvaldo M.,Hirotsune Shinji,Wynshaw-Boris Anthony,Dobyns William B.,Ledbetter David H.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

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3. 14-3-3 epsilon has no homology to LIS1 and lies telomeric to it on chromosome 17p13.3 outside the Miller-Dieker syndrome chromosome region;Chong;Genome Res,1996

4. A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3;Chong;Hum Mol Genet,1997

5. Large genomic duplicons map to sites of instability in the Prader-Willi/Angelman syndrome chromosome region (15q11–q13);Christian;Hum Mol Genet,1999

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