Publisher： Karger
E-ISSN： 1661-8777|1|4|176-184
ISSN： 1661-8769
Source： Molecular Syndromology, Vol.1, Iss.4, 2010-11, pp. : 176-184
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
Complex Phenotype Associated with 17q21.31 Microdeletion
Molecular Syndromology, Vol. 4, Iss. 6, 2013-08 ,pp. :
Access to resources
Recommend
American Journal Of Medical Genetics Part A, Vol. 167, Iss. 12, 2015-12 ,pp. :
Microdeletion 2q23.3q24.1: Exploring genotype‐phenotype correlations
CONGENITAL ANOMALIES, Vol. 55, Iss. 2, 2015-05 ,pp. :
By Christian Susan L. Fantes Judy A. Mewborn Stephanie K. Huang Bing Ledbetter David H. Ledbetter D.H. Nicholls R.D. Jiang Y. Webb T. Pettigrew A.L. Clayton-Smith J. Repetto G.M. Browne C.E. Robinson W.P. Schinzel A.A. Long F.L. Knoll J.H. Kuwano A. Mutirangura A. Christian S.L. Leana-Cox J. Crolla J.A. Huang B. Wandstrat A.E. Flejter W.L. Cook E.H. Donlon T.A. Tantravahi U. Buiting K. Buiting K. Ji Y. Lehman A.L. Nagase T. Christian S.L. Eichler E.E. Yunis J.J. Jauch A. Luke S. Wienberg J. Sutcliffe J.S. Kumar S. Schuler G.D. Kawasaki K. Allikmets R. Lupski J. Cooper D. Purandare S.M. Lupski J.R. Pentao L. Reiter L.T. Ballabio A. Yen P.H. Lakich D. Bondeson M.L. Small K. Small K. Lewis S.M. Konrad M. Lehrman M.A. Carrozzo R. Chen K.S. Lowery M.C. Nickerson E. Budarf M.L. Osbourne L.R. Perez Jurado L.A. Perez Jurado L.A. Morrow B. Edelmann L. McTaggert K.E. Tomlinson I.M. Nagaoka H. Purandare S.M. Regnier V. Kehrer-Sawatzki H. Ritchie R.J. Chong S.S. Finelli P. Trask B.J. van den Engh G.
Human Molecular Genetics, Vol. 8, Iss. 6, 1999-06 ,pp. :
Familial 5q12.3 Microdeletion: Evidence for a Locus Associated with Epilepsy
Molecular Syndromology, Vol. 8, Iss. 2, 2017-01 ,pp. :