Uniparental disomy with normal phenotype
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference5 articles.
1. Uniparental disomy 15 resulting from correction of an initial trisomy 15;Purvis-Smith;Am J Hum Genet,1992
2. Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy;Cassidy;Am J Hum Genet,1992
3. Dinucleotide repeat polymorphisms at the D16S260, D16S261, D16S265, D16S266 and D16S267 loci;Weber;Nucleic Acids Res,1990
4. Isolation and characterisation of (AC)n microsatellite genetic markers from human chromosome 16;Thompson;Genomics,1992
5. Confirmation of CVS mosaicism in term placentae and high frequency of intrauterine growth retardation association with confined placental mosaicism;Kalousek;Prenat Diagn,1991
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2. Postnatal follow-up of prenatally diagnosed trisomy 16 mosaicism;Prenatal Diagnosis;2006
3. Variable outcomes in mosaic trisomy 16: five case reports and literature analysis;Prenatal Diagnosis;2006
4. Sex-specific chromosome instability in early human development;American Journal of Medical Genetics Part A;2005
5. Uniparental disomy (UPD) other than 15: Phenotypes and bibliography updated;American Journal of Medical Genetics Part A;2005
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