Literature DB >> 1682673

Molecular cytogenetics of Prader-Willi and Angelman syndromes.

M G Butler, M A Greenstein.   

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Year:  1991        PMID： 1682673      PMCID： PMC5493389          DOI： 10.1016/0140-6736(91)92145-r

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  2 in total

1.  Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion.

Authors:  J H Knoll; R D Nicholls; R E Magenis; J M Graham; M Lalande; S A Latt
Journal:  Am J Med Genet       Date:  1989-02

2.  Parental origin of chromosome 15 deletion in Prader-Willi syndrome.

Authors:  M G Butler; C G Palmer
Journal:  Lancet       Date:  1983-06-04       Impact factor: 79.321
  2 in total
  3 in total

1.  High resolution chromosome analysis and fluorescence in situ hybridization in patients referred for Prader-Willi or Angelman syndrome.

Authors:  M G Butler
Journal:  Am J Med Genet       Date:  1995-05-08

2.  Are specific short arm variants or heteromorphisms over-represented in the chromosome 15 deletion in Angelman or Prader-Willi syndrome patients?

Authors:  M G Butler
Journal:  Am J Med Genet       Date:  1994-03-01

3.  Molecular study of chromosome 15 in 22 patients with Angelman syndrome.

Authors:  J Beuten; K Mangelschots; I Buntinx; P Coucke; O F Brouwer; R C Hennekam; C Van Broeckhoven; P J Willems
Journal:  Hum Genet       Date:  1993-01       Impact factor: 4.132
  3 in total

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