Adrenal hypoplasia congenita with phenotypic features suggestive of neurofibromatosis type 1 among three African-American brothers.
Publication
, Journal Article
Balikcioglu, PG; Gómez, R; Vargas, A; Aradhya, S; Messiaen, LM; Lacassie, Y
Published in: Am J Med Genet A
August 2013
Duke Scholars
Published In
Am J Med Genet A
DOI
EISSN
1552-4833
Publication Date
August 2013
Volume
161A
Issue
8
Start / End Page
2105 / 2107
Location
United States
Related Subject Headings
- Siblings
- Sequence Deletion
- Phenotype
- Neurofibromatosis 1
- Male
- Infant
- Hypoadrenocorticism, Familial
- Humans
- Genetic Diseases, X-Linked
- Diagnosis, Differential
Citation
APA
Chicago
ICMJE
MLA
NLM
Balikcioglu, P. G., Gómez, R., Vargas, A., Aradhya, S., Messiaen, L. M., & Lacassie, Y. (2013). Adrenal hypoplasia congenita with phenotypic features suggestive of neurofibromatosis type 1 among three African-American brothers. Am J Med Genet A, 161A(8), 2105–2107. https://doi.org/10.1002/ajmg.a.36031
Balikcioglu, Pinar Gumus, Ricardo Gómez, Alfonso Vargas, Swaroop Aradhya, Ludwine M. Messiaen, and Yves Lacassie. “Adrenal hypoplasia congenita with phenotypic features suggestive of neurofibromatosis type 1 among three African-American brothers.” Am J Med Genet A 161A, no. 8 (August 2013): 2105–7. https://doi.org/10.1002/ajmg.a.36031.
Balikcioglu PG, Gómez R, Vargas A, Aradhya S, Messiaen LM, Lacassie Y. Adrenal hypoplasia congenita with phenotypic features suggestive of neurofibromatosis type 1 among three African-American brothers. Am J Med Genet A. 2013 Aug;161A(8):2105–7.
Balikcioglu, Pinar Gumus, et al. “Adrenal hypoplasia congenita with phenotypic features suggestive of neurofibromatosis type 1 among three African-American brothers.” Am J Med Genet A, vol. 161A, no. 8, Aug. 2013, pp. 2105–07. Pubmed, doi:10.1002/ajmg.a.36031.
Balikcioglu PG, Gómez R, Vargas A, Aradhya S, Messiaen LM, Lacassie Y. Adrenal hypoplasia congenita with phenotypic features suggestive of neurofibromatosis type 1 among three African-American brothers. Am J Med Genet A. 2013 Aug;161A(8):2105–2107.
Published In
Am J Med Genet A
DOI
EISSN
1552-4833
Publication Date
August 2013
Volume
161A
Issue
8
Start / End Page
2105 / 2107
Location
United States
Related Subject Headings
- Siblings
- Sequence Deletion
- Phenotype
- Neurofibromatosis 1
- Male
- Infant
- Hypoadrenocorticism, Familial
- Humans
- Genetic Diseases, X-Linked
- Diagnosis, Differential