Publisher： Karger
E-ISSN： 1661-8777|2|3-5|164-170
ISSN： 1661-8769
Source： Molecular Syndromology, Vol.2, Iss.3-5, 2012-04, pp. : 164-170
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
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. :
Access to resources
Recommend
Clinical and Genetic Heterogeneity of the 15q13.3 Microdeletion Syndrome
Molecular Syndromology, Vol. 6, Iss. 5, 2015-0 ,pp. :
Microdeletion 2q23.3q24.1: Exploring genotype‐phenotype correlations
CONGENITAL ANOMALIES, Vol. 55, Iss. 2, 2015-05 ,pp. :
Interstitial deletion 5q14.3q21.3 associated with lethal epilepsy
American Journal Of Medical Genetics Part A, Vol. 167, Iss. 4, 2015-04 ,pp. :