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Prenatal genetic diagnosis of Neu-Laxova syndrome.

Publication ,  Journal Article
Wood, AM; Mottola, AT; Rhee, EH; Kuller, JA
Published in: J Obstet Gynaecol
April 2018

Duke Scholars

Published In

J Obstet Gynaecol

DOI

EISSN

1364-6893

Publication Date

April 2018

Volume

38

Issue

3

Start / End Page

413 / 414

Location

England

Related Subject Headings

  • Young Adult
  • Ultrasonography, Prenatal
  • Prenatal Diagnosis
  • Point Mutation
  • Phosphoglycerate Dehydrogenase
  • Pedigree
  • Obstetrics & Reproductive Medicine
  • Nuchal Translucency Measurement
  • Microcephaly
  • Limb Deformities, Congenital
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Wood, A. M., Mottola, A. T., Rhee, E. H., & Kuller, J. A. (2018). Prenatal genetic diagnosis of Neu-Laxova syndrome. J Obstet Gynaecol, 38(3), 413–414. https://doi.org/10.1080/01443615.2017.1343811
Wood, Amber M., Amy T. Mottola, Eleanor H. Rhee, and Jeffrey A. Kuller. “Prenatal genetic diagnosis of Neu-Laxova syndrome.J Obstet Gynaecol 38, no. 3 (April 2018): 413–14. https://doi.org/10.1080/01443615.2017.1343811.
Wood AM, Mottola AT, Rhee EH, Kuller JA. Prenatal genetic diagnosis of Neu-Laxova syndrome. J Obstet Gynaecol. 2018 Apr;38(3):413–4.
Wood, Amber M., et al. “Prenatal genetic diagnosis of Neu-Laxova syndrome.J Obstet Gynaecol, vol. 38, no. 3, Apr. 2018, pp. 413–14. Pubmed, doi:10.1080/01443615.2017.1343811.
Wood AM, Mottola AT, Rhee EH, Kuller JA. Prenatal genetic diagnosis of Neu-Laxova syndrome. J Obstet Gynaecol. 2018 Apr;38(3):413–414.

Published In

J Obstet Gynaecol

DOI

EISSN

1364-6893

Publication Date

April 2018

Volume

38

Issue

3

Start / End Page

413 / 414

Location

England

Related Subject Headings

  • Young Adult
  • Ultrasonography, Prenatal
  • Prenatal Diagnosis
  • Point Mutation
  • Phosphoglycerate Dehydrogenase
  • Pedigree
  • Obstetrics & Reproductive Medicine
  • Nuchal Translucency Measurement
  • Microcephaly
  • Limb Deformities, Congenital