
Hypereosinophilic syndrome and hemimelia in a patient with chromosome 6p22.3 deletion.
Publication
, Journal Article
Ladinsky, HT; Elizalde, A; Schickler, R; Dees, PB; Crenshaw, ML; Sleasman, JW
Published in: Pediatr Allergy Immunol
August 2014
Duke Scholars
Published In
Pediatr Allergy Immunol
DOI
EISSN
1399-3038
Publication Date
August 2014
Volume
25
Issue
5
Start / End Page
500 / 503
Location
England
Related Subject Headings
- Male
- Infant, Newborn
- Infant
- Hypereosinophilic Syndrome
- Humans
- Ectromelia
- Chromosomes, Human, Pair 6
- Chromosome Deletion
- Allergy
- Abnormalities, Multiple
Citation
APA
Chicago
ICMJE
MLA
NLM
Ladinsky, H. T., Elizalde, A., Schickler, R., Dees, P. B., Crenshaw, M. L., & Sleasman, J. W. (2014). Hypereosinophilic syndrome and hemimelia in a patient with chromosome 6p22.3 deletion. Pediatr Allergy Immunol, 25(5), 500–503. https://doi.org/10.1111/pai.12213
Ladinsky, Hava T., Araceli Elizalde, Robyn Schickler, Paola B. Dees, Melissa L. Crenshaw, and John W. Sleasman. “Hypereosinophilic syndrome and hemimelia in a patient with chromosome 6p22.3 deletion.” Pediatr Allergy Immunol 25, no. 5 (August 2014): 500–503. https://doi.org/10.1111/pai.12213.
Ladinsky HT, Elizalde A, Schickler R, Dees PB, Crenshaw ML, Sleasman JW. Hypereosinophilic syndrome and hemimelia in a patient with chromosome 6p22.3 deletion. Pediatr Allergy Immunol. 2014 Aug;25(5):500–3.
Ladinsky, Hava T., et al. “Hypereosinophilic syndrome and hemimelia in a patient with chromosome 6p22.3 deletion.” Pediatr Allergy Immunol, vol. 25, no. 5, Aug. 2014, pp. 500–03. Pubmed, doi:10.1111/pai.12213.
Ladinsky HT, Elizalde A, Schickler R, Dees PB, Crenshaw ML, Sleasman JW. Hypereosinophilic syndrome and hemimelia in a patient with chromosome 6p22.3 deletion. Pediatr Allergy Immunol. 2014 Aug;25(5):500–503.

Published In
Pediatr Allergy Immunol
DOI
EISSN
1399-3038
Publication Date
August 2014
Volume
25
Issue
5
Start / End Page
500 / 503
Location
England
Related Subject Headings
- Male
- Infant, Newborn
- Infant
- Hypereosinophilic Syndrome
- Humans
- Ectromelia
- Chromosomes, Human, Pair 6
- Chromosome Deletion
- Allergy
- Abnormalities, Multiple