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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

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Chicago
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MLA
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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.
Journal cover image

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