Publisher： Karger
E-ISSN： 1661-8777|2|2|72-75
ISSN： 1661-8769
Source： Molecular Syndromology, Vol.2, Iss.2, 2011-12, pp. : 72-75
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
Recurrent duplications of 17q12 associated with variable phenotypes
American Journal Of Medical Genetics Part A, Vol. 167, Iss. 12, 2015-12 ,pp. :
Access to resources
Recommend
Characterization of a recurrent 15q24 microdeletion syndrome
By Sharp Andrew J. Selzer Rebecca R. Veltman Joris A. Gimelli Stefania Gimelli Giorgio Striano Pasquale Coppola Antonietta Regan Regina Price Sue M. Knoers Nine V. Eis Peggy S. Brunner Han G. Hennekam Raoul C. Knight Samantha J.L. de Vries Bert B.A. Zuffardi Orsetta Eichler Evan E.
Human Molecular Genetics, Vol. 16, Iss. 5, 2007-03 ,pp. :
Complex Phenotype Associated with 17q21.31 Microdeletion
Molecular Syndromology, Vol. 4, Iss. 6, 2013-08 ,pp. :