Author:
Slavin Thomas P.,Lazebnik Noam,Clark Dinah M.,Vengoechea Jaime,Cohen Leslie,Kaur Maninder,Konczal Laura,Crowe Carol A.,Corteville Jane E.,Nowaczyk Malgorzata J.,Byrne Janice L.,Jackson Laird G.,Krantz Ian D.
Subject
Genetics(clinical),Genetics
Reference19 articles.
1. Sotos Syndrome;Baujat;Orphanet J Rare Dis,2007
2. Familial de Lange syndrome. Report of three cases in a sibship;Beratis;Clin Genet,1971
3. Perinatal lethal osteogenesis imperfecta (OI type II): A biochemically heterogeneous disorder usually due to new mutations in the genes for type I collagen;Byers;Am J Hum Genet,1988
4. Mutations in cohesin complex members SMC3 and SMC1A cause a mild variant of Cornelia de Lange syndrome with predominant mental retardation;Deardorff;Am J Hum Genet,2007
5. Inherited aneuploidy: Germline mosaicism;Delhanty;Cytogenet Genome Res,2011
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