Author： Veerakul G.
Publisher： Oxford University Press
ISSN： 1460-2083
Source： Human Molecular Genetics, Vol.11, Iss.3, 2002-02, pp. : 337-345
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
Related content
Human Heredity, Vol. 50, Iss. 3, 2000-02 ,pp. :
Access to resources
Recommend
By Kelberman D. Tyson J. Chandler D. McInerney A. Slee J. Albert D. Aymat A. Botma M. Calvert M. Goldblatt J. Haan E. Laing N. Lim J. Malcolm S. Singer S. Winter R. Bitner-Glindzicz M.
Human Genetics, Vol. 109, Iss. 6, 2001-12 ,pp. :
X-linked cataract and Nance-Horan syndrome are allelic disorders
By Coccia Margherita Brooks Simon P. Webb Tom R. Christodoulou Katja Wozniak Izabella O. Murday Victoria Balicki Martha Yee Harris A. Wangensteen Teresia Riise Ruth Saggar Anand K. Park Soo-Mi Kanuga Naheed Francis Peter J. Maher Eamonn R. Moore Anthony T. Russell-Eggitt Isabelle M. Hardcastle Alison J.
Human Molecular Genetics, Vol. 18, Iss. 14, 2009-07 ,pp. :
Understanding the molecular basis of fragile X syndrome
Human Molecular Genetics, Vol. 9, Iss. 6, 2000-04 ,pp. :
Exploring the molecular basis of Bardet–Biedl syndrome
By Katsanis N.
Human Molecular Genetics, Vol. 10, Iss. 20, 2001-10 ,pp. :