Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequences
- 1 March 1990
- Vol. 6 (3), 521-527
- https://doi.org/10.1016/0888-7543(90)90481-9
Abstract
No abstract availableThis publication has 24 references indexed in Scilit:
- Similar molecular deletions on chromosome 15q11.2 are encountered in both the Prader-Willi and Angelman syndromesHuman Genetics, 1988
- Construction of a chromosome 15-specific linking library and identification of potential gene sequences*1Genomics, 1988
- Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locusHuman Genetics, 1987
- A pipette method for rapid karyotyping in prenatal diagnosisPrenatal Diagnosis, 1986
- Clinical and cytogenetic survey of 39 individuals with Prader‐Labhart‐Willi syndromeAmerican Journal of Medical Genetics, 1986
- A technique for radiolabeling DNA restriction endonuclease fragments to high specific activityAnalytical Biochemistry, 1984
- Inhibitory effect of ethidium bromide on mitotic chromosome condensation and its application to high-resolution chromosome bandingCytogenetic and Genome Research, 1984
- Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainmentHuman Genetics, 1983
- Base sequence studies of 300 nucleotide renatured repeated human DNA clonesJournal of Molecular Biology, 1981
- ‘Puppet’ Children A Report on Three CasesDevelopmental Medicine and Child Neurology, 1965