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European Journal of Human Genetics : EJHG|September 29, 2011
De novo deletions and duplications detected by array CGH: a study of parental origin in relation to mechanisms of formation and size of imbalanceCharlene Sibbons, Joan K Morris, John A Crolla, et al.American Journal of Medical Genetics. Part A|February 14, 2006
Mosaic trisomy 6 and maternal uniparental disomy 6 in a 23-week gestation fetus with atrioventricular septal defectAnnette E Cockwell, Samantha J Baker, Margaret Connarty, et al.Lancet (London, England)|July 12, 2005
Prenatal detection of Down's syndrome by rapid aneuploidy testing for chromosomes 13, 18, and 21 by FISH or PCR without a full karyotype: a cytogenetic risk assessmentAllan Caine, A Edna Maltby, C Anthony Parkin, et al.American Journal of Medical Genetics. Part A|July 17, 2010
Investigation of 90 patients referred for molecular cytogenetic analysis using aCGH uncovers previously unsuspected anomalies of imprintingRebecca L Poole, Emma Baple, John A Crolla, et al.Plos One|October 2, 2012
Evaluation of a novel assay for detection of the fetal marker RASSF1A: facilitating improved diagnostic reliability of noninvasive prenatal diagnosisHelen E White, Carolyn L Dent, Victoria J Hall, et al.Prenatal Diagnosis|August 29, 2013
The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literatureJonathan L A Callaway, Lisa G Shaffer, Lyn S Chitty, et al.European Journal of Human Genetics : EJHG|August 25, 2005
Molecular cytogenetic analyses of breakpoints in apparently balanced reciprocal translocations carried by phenotypically normal individualsJulia Baptista, Elena Prigmore, Susan M Gribble, et al.Journal of Medical Genetics|July 30, 2009
De novo apparently balanced translocations in man are predominantly paternal in origin and associated with a significant increase in paternal ageN Simon Thomas, Joan K Morris, Julia Baptista, et al.European Journal of Medical Genetics|October 12, 2010
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 syndromeSwati Naik, Elliott Riordan-Eva, N Simon Thomas, et al.European Journal of Pediatric Surgery : Official Journal of Austrian Association of Pediatric Surgery ... [Et Al] = Zeitschrift Fur Kinderchirurgie|April 21, 2012
The use of mouth brushings for screening girls who present with inguinal hernia for complete androgen insensitivity syndromeShakeel M Rahman, Nigel J Hall, John A Crolla, et al.Pageof 5