doi: 10.1016/0140-6736(91)90652-6.
Genomic imprinting in an Angelman and Prader-Willi translocation family
- PMID: 1679180
- DOI: 10.1016/0140-6736(91)90652-6
Item in Clipboard
Genomic imprinting in an Angelman and Prader-Willi translocation family
Lancet.
.
No abstract available
Comment in
-
Molecular cytogenetics of Prader-Willi and Angelman syndromes.Lancet. 1991 Nov 16;338(8777):1276. doi: 10.1016/0140-6736(91)92145-r. Lancet. 1991. PMID: 1682673 Free PMC article. No abstract available.
Similar articles
-
Deletions of proximal 15q without Prader-Willi syndrome.Am J Med Genet. 1987 Dec;28(4):813-20. doi: 10.1002/ajmg.1320280405. Am J Med Genet. 1987. PMID: 3688019
-
Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequences.Genomics. 1990 Mar;6(3):521-7. doi: 10.1016/0888-7543(90)90481-9. Genomics. 1990. PMID: 2328991
-
[Chromosome aberrations in Prader-Willi-Labhart syndrome--critical review, documented by 4 unusual cases].Klin Padiatr. 1987 Sep-Oct;199(5):329-35. doi: 10.1055/s-2008-1026814. Klin Padiatr. 1987. PMID: 3316824 Review. German.
-
Prader-Willi and Angelman syndromes: update on genetic mechanisms and diagnostic complexities.Curr Opin Neurol. 1999 Apr;12(2):149-54. doi: 10.1097/00019052-199904000-00004. Curr Opin Neurol. 1999. PMID: 10226746 Review.
-
Prader-Willi syndrome and Angelman syndrome in cousins from a family with a translocation between chromosomes 6 and 15.N Engl J Med. 1992 Mar 19;326(12):807-11. doi: 10.1056/NEJM199203193261206. N Engl J Med. 1992. PMID: 1538725 No abstract available.
Cited by
-
Angelman syndrome: a review of the clinical and genetic aspects.J Med Genet. 2003 Feb;40(2):87-95. doi: 10.1136/jmg.40.2.87. J Med Genet. 2003. PMID: 12566516 Free PMC article. Review.
-
Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy.Am J Hum Genet. 1992 Oct;51(4):701-8. Am J Hum Genet. 1992. PMID: 1357962 Free PMC article.
-
Molecular mechanisms in Angelman syndrome: a survey of 93 patients.J Med Genet. 1993 Nov;30(11):895-902. doi: 10.1136/jmg.30.11.895. J Med Genet. 1993. PMID: 7905534 Free PMC article.
-
Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.Hum Mol Genet. 1993 Feb;2(2):143-51. doi: 10.1093/hmg/2.2.143. Hum Mol Genet. 1993. PMID: 8499903 Free PMC article.
-
Linkage analysis with chromosome 15q11-13 markers shows genomic imprinting in familial Angelman syndrome.J Med Genet. 1992 Dec;29(12):853-7. doi: 10.1136/jmg.29.12.853. J Med Genet. 1992. PMID: 1362220 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical
