Exome sequencing enables diagnosis of X-linked hypohidrotic ectodermal dysplasia in patient with eosinophilic esophagitis and severe atopy

MLA

Bhavi P. Modi, et al. “Exome Sequencing Enables Diagnosis of X-Linked Hypohidrotic Ectodermal Dysplasia in Patient with Eosinophilic Esophagitis and Severe Atopy.” Allergy, Asthma & Clinical Immunology, vol. 17, no. 1, Jan. 2021, pp. 1–6. EBSCOhost, https://doi.org/10.1186/s13223-021-00510-z.

APA

Bhavi P. Modi, Kate L. Del Bel, Susan Lin, Mehul Sharma, Phillip A. Richmond, Clara D. M. van Karnebeek, Edmond S. Chan, Vishal Avinashi, Wingfield E. Rehmus, Catherine M. Biggs, Wyeth W. Wasserman, & Stuart E. Turvey. (2021). Exome sequencing enables diagnosis of X-linked hypohidrotic ectodermal dysplasia in patient with eosinophilic esophagitis and severe atopy. Allergy, Asthma & Clinical Immunology, 17(1), 1–6. https://doi.org/10.1186/s13223-021-00510-z

Chicago

Bhavi P. Modi, Kate L. Del Bel, Susan Lin, Mehul Sharma, Phillip A. Richmond, Clara D. M. van Karnebeek, Edmond S. Chan, et al. 2021. “Exome Sequencing Enables Diagnosis of X-Linked Hypohidrotic Ectodermal Dysplasia in Patient with Eosinophilic Esophagitis and Severe Atopy.” Allergy, Asthma & Clinical Immunology 17 (1): 1–6. doi:10.1186/s13223-021-00510-z.