A molecular deletion study with southern hybridization on typical Prader-Willi syndrome (PWS) patients with various chromosome abnormalities involving 15q11–12 and on an atypical PWS patient with apparently normal karyotype

This publication has 29 references indexed in Scilit:

• Neonatal diagnosis of Prader‐Willi syndrome and its implications
  American Journal of Medical Genetics, 1987
• Recurrence risk in Prader-Willi syndrome
  American Journal of Medical Genetics, 1987
• Localization of the human prealbumin gene to 18p11.1-q12.3 by gene dose effect study of Southern blot hybridization
  Journal of Human Genetics, 1986
• Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome.
  Proceedings of the National Academy of Sciences, 1986
• Clinical and cytogenetic survey of 39 individuals with Prader‐Labhart‐Willi syndrome
  American Journal of Medical Genetics, 1986
• Duplication or insertion in 15q11–13 associated with mental retardation ‐short stature and obesity ‐ Prader‐Willi or Cohen syndrome?
  Clinical Genetics, 1984
• Cytogenetic studies of familial Prader-Willi syndrome
  Human Genetics, 1984
• PRADER-WILLI SYNDROME AND PRENATAL DIAGNOSIS
  The Lancet, 1983
• Parental origin of de novo chromosome rearrangements
  Human Genetics, 1980
• Some mapping theorems for the numerical range
  Proceedings of the Japan Academy, Series A, Mathematical Sciences, 1965