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Results: 1-2 |
Results: 2
Mapping of Deletion and Translocation Breakpoints in 1q44 Implicates the Serine/Threonine Kinase AKT3 in Postnatal Microcephaly and Agenesis of the Corpus Callosum
Authors: Boland, Elena Clayton-Smith, Jill Woo, Victoria G. McKee, Shane Manson, Forbes D.C. Medne, Livija Zackai, Elaine Swanson, Eric A. Fitzpatrick, David Millen,Kathleen J. Sherr, Elliott H. Dobyns, William B Black, Graeme C.M.
Citation: Boland, Elena et al., Mapping of Deletion and Translocation Breakpoints in 1q44 Implicates the Serine/Threonine Kinase AKT3 in Postnatal Microcephaly and Agenesis of the Corpus Callosum, American journal of human genetics , 81(2), 2007, pp. 292-303
Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes
Authors: Delio, Maria Guo, Tingwei McDonald-McGinn, Donna M. Zackai, Elaine
Citation: Delio, Maria et al., Enhanced Maternal Origin of the 22q11.2 Deletion in Velocardiofacial and DiGeorge Syndromes, American journal of human genetics (Online) AJHG , 92(3), 2013, pp. 439-447
Risultati: 1-2 |