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