Chromosome 7p - syndrome: Craniosynostosis with preservation of region 7p2
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference24 articles.
1. Interstitial deletion of the short arm of chromosome 7 without craniosynostosis
2. Partial monosomy 7 with interstitial deletions in two infants with differing congenital abnormalities.
3. Terminal 7p deletion and 1;7 translocation associated with craniosynostosis
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1. A novel de novo deletion of chromosome 7 [46,XX,del(7)(p14.2 p15.1)] in a child with feeding problems;Gene;2012-07
2. Large de novo deletion of 7p15.1 to 7p12.1 involving the imprinted gene GRB10 associated with a complex phenotype including features of Beckwith Wiedemann syndrome;European Journal of Medical Genetics;2011-01
3. Greig cephalopolysyndactyly syndrome: altered phenotype of a microdeletion syndrome due to the presence of a cytogenetic abnormality;Clinical Genetics;2008-06-28
4. Mosaic 22q11.2 microdeletion syndrome: diagnosis and clinical manifestations of two cases;Molecular Cytogenetics;2008
5. Partial Trisomy 3p and Monosomy 7p Associated with Tetralogy of Fallot and Infantile Seizure;Taiwanese Journal of Obstetrics and Gynecology;2007-09
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