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Prenatal Diagnosis|January 15, 2022
A framework for reporting secondary and incidental findings in prenatal sequencing: When and for whom?Danya Vears, David J AmorHuman Reproduction (Oxford, England)|August 16, 2008
A review of known imprinting syndromes and their association with assisted reproduction technologiesDavid J Amor, Jane HallidayHuman Reproduction (Oxford, England)|January 29, 2008
PGD gender selection for non-Mendelian disorders with unequal sex incidenceDavid J Amor, Carolyn CameronClinical Chemistry|December 31, 2015
Identification of Males with Cryptic Fragile X Alleles by Methylation-Specific Quantitative Melt AnalysisSolange M Aliaga, Howard R Slater, David Francis, et al.Epigenomics|October 4, 2024
Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newbornsMohammed Alshawsh, Melissa Wake, Jozef Gecz, et al.American Journal of Medical Genetics. Part A|December 14, 2006
Obesity, hypothyroidism, craniosynostosis, cardiac hypertrophy, colitis, and developmental delay: a novel syndromeTiong Yang Tan, David J AmorJournal of Paediatrics and Child Health|June 18, 2024
Intellectual disability: A potentially treatable conditionSarah E Donoghue, David J AmorJournal of Paediatrics and Child Health|August 24, 2006
Tumour surveillance in Beckwith-Wiedemann syndrome and hemihyperplasia: a critical review of the evidence and suggested guidelines for local practiceTiong Y Tan, David J AmorInternational Journal of Molecular Sciences|October 22, 2020
DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X SyndromeClaudine M Kraan, Emma K Baker, Marta Arpone, et al.International Journal of Molecular Sciences|August 14, 2019
Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X TestingMichael Field, Tracy Dudding-Byth, Marta Arpone, et al.Pageof 27