Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome-Reference-Cited by-同舟云学术

Deletions Involving Long-Range Conserved Nongenic Sequences Upstream and Downstream of FOXL2 as a Novel Disease-Causing Mechanism in Blepharophimosis Syndrome

Published:2005-08 Issue:2 Volume:77 Page:205-218
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Beysen D.,Raes J.,Leroy B.P.,Lucassen A.,Yates J.R.W.,Clayton-Smith J.,Ilyina H.,Brooks S. Sklower,Christin-Maitre S.,Fellous M.,Fryns J.P.,Kim J.R.,Lapunzina P.,Lemyre E.,Meire F.,Messiaen L.M.,Oley C.,Splitt M.,Thomson J.,Peer Y. Van de,Veitia R.A.,De Paepe A.,De Baere E.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference41 articles.

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2. Ultraconserved elements in the human genome;Bejerano;Science,2004

3. Mutations in the coding region of the FOXL2 gene are not a major cause of idiopathic premature ovarian failure;Bodega;Mol Hum Reprod,2004

4. Mutational analysis of forkhead transcriptional factor 2 (FOXL2) in Korean patients with blepharophimosis-ptosis-epicanthus inversus syndrome;Cha;Clin Genet,2003

5. Structure, evolution and expression of the FOXL2 transcription unit;Cocquet;Cytogenet Genome Res,2003

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