High resolution chromosome analysis and fluorescence in situ hybridization in patients referred for Prader‐Willi or Angelman syndrome
- 8 May 1995
- journal article
- letter
- Published by Wiley in American Journal of Medical Genetics
- Vol. 56 (4) , 420-422
- https://doi.org/10.1002/ajmg.1320560414
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Comparison of high resolution chromosome banding and fluorescence in situ hybridization (FISH) for the laboratory evaluation of Prader‐Willi syndrome and angelman syndromeAmerican Journal of Medical Genetics, 1994
- Are specific short arm variants or heteromorphisms over‐represented in the chromosome 15 deletion in Angelman or Prader‐Willi syndrome patients?American Journal of Medical Genetics, 1994
- Cytogenetic and molecular analysis in Angelman syndromeAmerican Journal of Medical Genetics, 1993
- Small nuclear ribonucleoprotein polypeptide N (SNRPN), an expressed gene in the Prader–Willi syndrome critical regionNature Genetics, 1992
- The Frequency of Uniparental Disomy in Prader-Willi SyndromeNew England Journal of Medicine, 1992
- Molecular cytogenetics of Prader-Willi and Angelman syndromesThe Lancet, 1991
- Prader‐Willi syndrome: Current understanding of cause and diagnosisAmerican Journal of Medical Genetics, 1990
- Genetic imprinting suggested by maternal heterodisomy in non-deletion Prader-Willi syndromeNature, 1989
- Clinical and cytogenetic survey of 39 individuals with Prader‐Labhart‐Willi syndromeAmerican Journal of Medical Genetics, 1986