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Common single-nucleotide polymorphisms in the BNC2, HOXD1 and MERIT40 regions contribute significantly to racial differences in ovarian cancer incidence

Publication ,  Journal Article
Berchuck, A; Pike, M; Schildkraut, J; Pearce, C
Published in: Gynecologic Oncology
March 2011

Duke Scholars

Published In

Gynecologic Oncology

DOI

ISSN

0090-8258

Publication Date

March 2011

Volume

120

Start / End Page

S7 / S7

Publisher

Elsevier BV

Related Subject Headings

  • Oncology & Carcinogenesis
  • 3215 Reproductive medicine
  • 3211 Oncology and carcinogenesis
  • 3202 Clinical sciences
  • 1114 Paediatrics and Reproductive Medicine
  • 1112 Oncology and Carcinogenesis
 

Citation

APA
Chicago
ICMJE
MLA
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Berchuck, A., Pike, M., Schildkraut, J., & Pearce, C. (2011). Common single-nucleotide polymorphisms in the BNC2, HOXD1 and MERIT40 regions contribute significantly to racial differences in ovarian cancer incidence. Gynecologic Oncology, 120, S7–S7. https://doi.org/10.1016/j.ygyno.2010.12.019
Berchuck, A., M. Pike, J. Schildkraut, and C. Pearce. “Common single-nucleotide polymorphisms in the BNC2, HOXD1 and MERIT40 regions contribute significantly to racial differences in ovarian cancer incidence.” Gynecologic Oncology 120 (March 2011): S7–S7. https://doi.org/10.1016/j.ygyno.2010.12.019.
Berchuck, A., et al. “Common single-nucleotide polymorphisms in the BNC2, HOXD1 and MERIT40 regions contribute significantly to racial differences in ovarian cancer incidence.” Gynecologic Oncology, vol. 120, Elsevier BV, Mar. 2011, pp. S7–S7. Crossref, doi:10.1016/j.ygyno.2010.12.019.
Berchuck A, Pike M, Schildkraut J, Pearce C. Common single-nucleotide polymorphisms in the BNC2, HOXD1 and MERIT40 regions contribute significantly to racial differences in ovarian cancer incidence. Gynecologic Oncology. Elsevier BV; 2011 Mar;120:S7–S7.
Journal cover image

Published In

Gynecologic Oncology

DOI

ISSN

0090-8258

Publication Date

March 2011

Volume

120

Start / End Page

S7 / S7

Publisher

Elsevier BV

Related Subject Headings

  • Oncology & Carcinogenesis
  • 3215 Reproductive medicine
  • 3211 Oncology and carcinogenesis
  • 3202 Clinical sciences
  • 1114 Paediatrics and Reproductive Medicine
  • 1112 Oncology and Carcinogenesis