Literature DB >> 3674119

Recurrence risk in Prader-Willi syndrome.

S B Cassidy.   

Abstract

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Year:  1987        PMID： 3674119     DOI： 10.1002/ajmg.1320280109

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


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  6 in total

1.  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

2.  Fenfluramine in Prader-Willi syndrome: a double blind, placebo controlled trial.

Authors:  M Selikowitz; J Sunman; A Pendergast; S Wright
Journal:  Arch Dis Child       Date:  1990-01       Impact factor: 3.791

Review 3.  The Prader-Willi syndrome.

Authors:  M D Donaldson; C E Chu; A Cooke; A Wilson; S A Greene; J B Stephenson
Journal:  Arch Dis Child       Date:  1994-01       Impact factor: 3.791

4.  Trisomy 15 with loss of the paternal 15 as a cause of Prader-Willi syndrome due to maternal disomy.

Authors:  S B Cassidy; L W Lai; R P Erickson; L Magnuson; E Thomas; R Gendron; J Herrmann
Journal:  Am J Hum Genet       Date:  1992-10       Impact factor: 11.025

5.  Prader-Willi syndrome: current understanding of cause and diagnosis.

Authors:  M G Butler
Journal:  Am J Med Genet       Date:  1990-03

Review 6.  Genomic imprinting: implications for behavioral genetics.

Authors:  M J Durcan; D Goldman
Journal:  Behav Genet       Date:  1993-03       Impact factor: 2.805
  6 in total

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