Isochromosome 15q of maternal origin in two Prader-Willi syndrome patients previously diagnosed erroneously as cytogenetic deletions
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference30 articles.
1. Monosomy for 21pter-q21: Case report and assignment of a DNA clone (Fr8-77) to the deleted segment
2. FUSION OF HOMOLOGOUS CHROMOSOMES (15q15q) AS CAUSE OF RECURRENT ABORTION
3. Dinucleotide repeat polymorphism at the D11S527 locus
4. Prader-Willi syndrome and Robertsonian translocations involving chromosome 15
5. Paternal uniparental disomy in a child with a balanced 15;15 translocation and Angelman syndrome
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1. The dilemma of diagnostic testing for Prader-Willi syndrome;Translational Pediatrics;2017-01
2. Mosaic isochromosome 15q and maternal uniparental isodisomy for chromosome 15 in a patient with morbid obesity and variant PWS-like phenotype;American Journal of Medical Genetics Part A;2013-05-17
3. Complex and segmental uniparental disomy updated;Journal of Medical Genetics;2008-06-04
4. A case described as translocation 15;15 revised: maternal 15 UPD, resulting from isochromosome 15, in a PWS patient;European Journal of Medical Genetics;2005-04
5. Sex-specific chromosome instability in early human development;American Journal of Medical Genetics Part A;2005
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