Calvarial mass as a presenting feature of neurofibromatosis type 2 in a pediatric patient.
Publication
, Journal Article
Narine, KY; Oh, CC; Fuchs, HE; Van Mater, D
Published in: Am J Med Genet A
January 2018
Duke Scholars
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Published In
Am J Med Genet A
DOI
EISSN
1552-4833
Publication Date
January 2018
Volume
176
Issue
1
Start / End Page
246 / 247
Location
United States
Related Subject Headings
- Treatment Outcome
- Tomography, X-Ray Computed
- Symptom Assessment
- Skull
- Phenotype
- Neurofibromatosis 2
- Male
- Magnetic Resonance Imaging
- Humans
- Genetic Testing
Citation
APA
Chicago
ICMJE
MLA
NLM
Narine, K. Y., Oh, C. C., Fuchs, H. E., & Van Mater, D. (2018). Calvarial mass as a presenting feature of neurofibromatosis type 2 in a pediatric patient. Am J Med Genet A, 176(1), 246–247. https://doi.org/10.1002/ajmg.a.38505
Narine, Kalindi Y., Christopher C. Oh, Herbert E. Fuchs, and David Van Mater. “Calvarial mass as a presenting feature of neurofibromatosis type 2 in a pediatric patient.” Am J Med Genet A 176, no. 1 (January 2018): 246–47. https://doi.org/10.1002/ajmg.a.38505.
Narine KY, Oh CC, Fuchs HE, Van Mater D. Calvarial mass as a presenting feature of neurofibromatosis type 2 in a pediatric patient. Am J Med Genet A. 2018 Jan;176(1):246–7.
Narine, Kalindi Y., et al. “Calvarial mass as a presenting feature of neurofibromatosis type 2 in a pediatric patient.” Am J Med Genet A, vol. 176, no. 1, Jan. 2018, pp. 246–47. Pubmed, doi:10.1002/ajmg.a.38505.
Narine KY, Oh CC, Fuchs HE, Van Mater D. Calvarial mass as a presenting feature of neurofibromatosis type 2 in a pediatric patient. Am J Med Genet A. 2018 Jan;176(1):246–247.
Published In
Am J Med Genet A
DOI
EISSN
1552-4833
Publication Date
January 2018
Volume
176
Issue
1
Start / End Page
246 / 247
Location
United States
Related Subject Headings
- Treatment Outcome
- Tomography, X-Ray Computed
- Symptom Assessment
- Skull
- Phenotype
- Neurofibromatosis 2
- Male
- Magnetic Resonance Imaging
- Humans
- Genetic Testing