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Volumn 112, Issue 6, 2002, Pages 962-967

Ectodermal dysplasia: Otolaryngologic manifestations and management

Author keywords

Hypohidrotic ectodermal dysplasia; Otolaryngologic manifestations odontotrichomelic syndrome; Witkop syndrome

Indexed keywords

ADULT; ALOPECIA; ARTICLE; CHILD; CLINICAL ARTICLE; CORNEA INJURY; DENTISTRY; DERMATOLOGY; DRY EYE; DYSPHAGIA; DYSPHONIA; ECZEMA; EPISTAXIS; FACIES; FEMALE; HEARING LOSS; HUMAN; HYPODONTIA; HYPOHIDROTIC ECTODERMAL DYSPLASIA; INFANT; MALE; MEDICAL GENETICS; OTITIS MEDIA; OTORHINOLARYNGOLOGY; PEDIATRIC HOSPITAL; PHARYNGITIS; PRIORITY JOURNAL; RETROSPECTIVE STUDY; RHINITIS; SYNDROME; X CHROMOSOME LINKED DISORDER;

EID: 0036276342     PISSN: 0023852X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00005537-200206000-00005     Document Type: Article
Times cited : (35)

References (11)
  • 11
    • 0032231350 scopus 로고    scopus 로고
    • Identification of a new splice form of the EDA 1 gene permits detection of nearly all X-linked hypohidrotic ectodermal dysplasia mutations
    • (1998) Am J Hum Genet , vol.63 , pp. 380-389
    • Monreal, A.W.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.