19q13 microdeletion syndrome: Further refining the critical region
Authors:
- Francesca ForzanoFFFrancesca Forzano
- Flavia NapoliFNFlavia Napoli
- Vera UlianaVUVera Uliana
- Michela MalacarneMMMichela Malacarne
- Chiara ViaggiCVChiara Viaggi
- Raffaella BloiseRBRaffaella Bloise
- Domenico CovielloDCDomenico Coviello
- Emilio Di MariaEMEmilio Di Maria
- Irene OlivieriIOIrene Olivieri
- Natascia Di IorgiNINatascia Di Iorgi
- Francesca FaravelliFFFrancesca Faravelli
- 1 June 2012
- journal article
- case report
- Published by Elsevier in European Journal of Medical Genetics
- Vol. 55 (6-7) , 429-432
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
- Rapid Sequence and Expression Divergence Suggest Selection for Novel Function in Primate-Specific KRAB-ZNF GenesMolecular Biology and Evolution, 2010
- Refining the critical region of the novel 19q13.11 microdeletion syndrome to 750 KbJournal of Medical Genetics, 2009
- 19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisationJournal of Medical Genetics, 2009
- Constitutional del(19)(q12q13.1) in a three-year-old girl with severe phenotypic abnormalities affecting multiple organ systemsAmerican Journal of Medical Genetics, 1998
- Comparative Analysis of a Conserved Zinc Finger Gene Cluster on Human Chromosome 19q and Mouse Chromosome 7Genomics, 1996