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Exclusion of maternal uniparental disomy of chromosome 14 in patients referred for Prader-Willi syndrome using a multiplex methylation polymerase chain reaction assay.

Publication ,  Journal Article
Dietz, LG; Wylie, AA; Rauen, KA; Murphy, SK; Jirtle, RL; Cotter, PD
Published in: J Med Genet
April 2003

Duke Scholars

Published In

J Med Genet

DOI

EISSN

1468-6244

Publication Date

April 2003

Volume

40

Issue

4

Start / End Page

e46

Location

England

Related Subject Headings

  • Uniparental Disomy
  • RNA, Long Noncoding
  • Proteins
  • Promoter Regions, Genetic
  • Prader-Willi Syndrome
  • Polymerase Chain Reaction
  • Male
  • Humans
  • Genetics & Heredity
  • Female
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Dietz, L. G., Wylie, A. A., Rauen, K. A., Murphy, S. K., Jirtle, R. L., & Cotter, P. D. (2003). Exclusion of maternal uniparental disomy of chromosome 14 in patients referred for Prader-Willi syndrome using a multiplex methylation polymerase chain reaction assay. J Med Genet, 40(4), e46. https://doi.org/10.1136/jmg.40.4.e46
Dietz, L. G., A. A. Wylie, K. A. Rauen, S. K. Murphy, R. L. Jirtle, and P. D. Cotter. “Exclusion of maternal uniparental disomy of chromosome 14 in patients referred for Prader-Willi syndrome using a multiplex methylation polymerase chain reaction assay.J Med Genet 40, no. 4 (April 2003): e46. https://doi.org/10.1136/jmg.40.4.e46.

Published In

J Med Genet

DOI

EISSN

1468-6244

Publication Date

April 2003

Volume

40

Issue

4

Start / End Page

e46

Location

England

Related Subject Headings

  • Uniparental Disomy
  • RNA, Long Noncoding
  • Proteins
  • Promoter Regions, Genetic
  • Prader-Willi Syndrome
  • Polymerase Chain Reaction
  • Male
  • Humans
  • Genetics & Heredity
  • Female