Literature DB >> 6134086

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

M G Butler, C G Palmer.   

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Year:  1983        PMID： 6134086      PMCID： PMC5510872          DOI： 10.1016/s0140-6736(83)92745-9

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


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  5 in total

1.  Prader-Willi syndrome. A resumé of 32 cases including an instance of affected first cousins, one of whom is of normal stature and intelligence.

Authors:  B D Hall; D W Smith
Journal:  J Pediatr       Date:  1972-08       Impact factor: 4.406

2.  Syndrome of hypotonia-hypomentia-hypogonadism-obesity (HHHO) or Prader-Willi syndrome.

Authors:  H Zellweger; H J Schneider
Journal:  Am J Dis Child       Date:  1968-05

3.  On the structure and polymorphism of the human chromosome no. 15.

Authors:  F Wachtler; R Musil
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

4.  Deletions of chromosome 15 as a cause of the Prader-Willi syndrome.

Authors:  D H Ledbetter; V M Riccardi; S D Airhart; R J Strobel; B S Keenan; J D Crawford
Journal:  N Engl J Med       Date:  1981-02-05       Impact factor: 91.245

5.  Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome.

Authors:  M G Butler; S G Kaler; P L Yu; F J Meaney
Journal:  Clin Genet       Date:  1982-12       Impact factor: 4.438
  5 in total
  68 in total

1.  Molecular analysis of patients with Wiedemann-Beckwith syndrome. II. Paternally derived disomies of chromosome 11.

Authors:  A Nyström; J E Cheetham; W Engström; P N Schofield
Journal:  Eur J Pediatr       Date:  1992-07       Impact factor: 3.183

2.  Angelman syndrome with a chromosomal inversion 15 inv(p11q13) accompanied by a deletion in 15q11q13.

Authors:  T Webb; J Clayton-Smith; X J Cheng; J H Knoll; M Lalande; M E Pembrey; S Malcolm
Journal:  J Med Genet       Date:  1992-12       Impact factor: 6.318

3.  Replication asynchrony between homologs 15q11.2: cytogenetic evidence for genomic imprinting.

Authors:  Y Izumikawa; K Naritomi; K Hirayama
Journal:  Hum Genet       Date:  1991-05       Impact factor: 4.132

4.  Molecular cytogenetics of Prader-Willi and Angelman syndromes.

Authors:  M G Butler; M A Greenstein
Journal:  Lancet       Date:  1991-11-16       Impact factor: 79.321

5.  The impact of imprinting: Prader-Willi syndrome resulting from chromosome translocation, recombination, and nondisjunction.

Authors:  S Toth-Fejel; S Olson; K Gunter; F Quan; J Wolford; B W Popovich; R E Magenis
Journal:  Am J Hum Genet       Date:  1996-05       Impact factor: 11.025

6.  Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndrome.

Authors:  O W Quarrell; R G Snell; M A Curtis; S H Roberts; P S Harper; D J Shaw
Journal:  J Med Genet       Date:  1991-04       Impact factor: 6.318

7.  Maternal origin of deletion 15q11-13 in 25/25 cases of Angelman syndrome.

Authors:  J C Smith; T Webb; M E Pembrey; M Nichols; S Malcolm
Journal:  Hum Genet       Date:  1992-02       Impact factor: 4.132

8.  Sudden cardiac death in a child affected by Prader-Willi syndrome.

Authors:  Cristoforo Pomara; Stefano D'Errico; Irene Riezzo; Gian Pio de Cillis; Vittorio Fineschi
Journal:  Int J Legal Med       Date:  2005-03-05       Impact factor: 2.686

Review 9.  Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.

Authors:  M G Mattei; N Souiah; J F Mattei
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

10.  Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient.

Authors:  Y Sun; R D Nicholls; M G Butler; S Saitoh; B E Hainline; C G Palmer
Journal:  Hum Mol Genet       Date:  1996-04       Impact factor: 6.150
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