Placental hypoplasia in maternal uniparental disomy for chromosome 7
- 17 January 2008
- journal article
- case report
- Published by Wiley in American Journal of Medical Genetics Part A
- Vol. 146A (4) , 514-516
- https://doi.org/10.1002/ajmg.a.32125
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Placental mesenchymal dysplasia associated with fetal overgrowth and mosaic deletion of the maternal copy of 11p15.5American Journal of Medical Genetics Part A, 2007
- Silver-Russell syndrome in a girl born after in vitro fertilization: partial hypermethylation at the differentially methylated region of PEG1/MESTJournal of Assisted Reproduction and Genetics, 2007
- Absence of a Paternally Inherited FOXP2 Gene in Developmental Verbal DyspraxiaAmerican Journal of Human Genetics, 2006
- Imprinted Genes, Placental Development and Fetal GrowthHormone Research in Paediatrics, 2006
- Complete maternal uniparental isodisomy of chromosome 4 in a subject with major depressive disorder detected by high density SNP genotyping arraysAmerican Journal Of Medical Genetics Part B-Neuropsychiatric Genetics, 2005
- The ubiquitin ligase Hyperplastic discs negatively regulateshedgehoganddecapentaplegicexpression by independent mechanismsDevelopment, 2002
- Erasing genomic imprinting memory in mouse clone embryos produced from day 11.5 primordial germ cellsDevelopment, 2002
- Silver-Russell syndrome: a dissection of the genetic aetiology and candidate chromosomal regionsJournal of Medical Genetics, 2001
- Post-Zygotic Origin of Complete Maternal Chromosome 7 Isodisomy and Consequent Loss of Placental PEG1/MEST ExpressionPlacenta, 2001
- Diagnosis of maternal uniparental disomy of chromosome 7 with a methylation specific PCR assayJournal of Medical Genetics, 2000