Refinement of the genetic cause of ATR-16-Reference-Cited by-同舟云学术

Refinement of the genetic cause of ATR-16

Published:2007-06-28 Issue:3-4 Volume:122 Page:283-292
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Harteveld Cornelis L.,Kriek Marjolein,Bijlsma Emilia K.,Erjavec Zoran,Balak Deepak,Phylipsen Marion,Voskamp Astrid,Capua Emmanora di,White Stefan J.,Giordano Piero C.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s00439-007-0399-y.pdf

Reference40 articles.

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3. Cardoso C, Timsit S, Villard L, Khrestchatisky M, Fontes M, Colleaux L (1998) Specific interaction between the XNP/ATR-X gene product and the SET domain of the human EZH2 protein. Hum Mol Genet 7:679–684

4. Cardoso C, Lutz Y, Mignon C, Compe E, Depetris D, Mattei MG, Fontes M, Colleaux L (2000) ATR-X mutations cause impaired nuclear location and altered DNA binding properties of the XNP/ATR-X protein. J Med Genet 37:746–751

5. Chong SS, Boehm CD, Higgs DR, Cutting GR (2000) Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia. Blood 95:360–362

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