Form of 15q proximal duplication appears to be a normal euchromatic variant

This publication has 9 references indexed in Scilit:

• Proximal 15q variant with normal phenotype in three unrelated individuals
  Clinical Genetics, 2008
• Absence of predictable phenotypic expression in proximal 15q duplications
  Clinical Genetics, 2008
• Proximal duplications of chromosome 15: clinical dilemmas
  Clinical Genetics, 2008
• Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome.
  Journal of Medical Genetics, 1993
• Method for sequential staining of GTL‐banded metaphases with fluorescent‐labeled chromosome‐specific paint probes
  American Journal of Medical Genetics, 1993
• Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11–q13): molecular diagnosis and mechanism of uniparental disomy
  Human Molecular Genetics, 1993
• Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader–Willi syndrome critical region
  Nature Genetics, 1992
• A second-generation linkage map of the human genome
  Nature, 1992
• Conference report: First international scientific workshop on Prader‐Willi Syndrome and Other Chromosome 15q Deletion Disorders
  American Journal of Medical Genetics, 1992