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Volumn 11, Issue 3, 2002, Pages 179-182

A severe case of oculo-ectodermal syndrome?

Author keywords

Oculo ectodermal syndrome

Indexed keywords

ANUS; ARTICLE; CASE REPORT; CLINICAL FEATURE; DEVELOPMENTAL DISORDER; FACE MALFORMATION; FEMALE; HUMAN; INFANT; LARYNGOMALACIA; MICROCEPHALY; NEW ZEALAND; OCULOECTODERMAL SYNDROME; PRIORITY JOURNAL; RECESSIVE INHERITANCE; ECTODERM; EYE MALFORMATION; GENETICS; MALE; MULTIPLE MALFORMATION SYNDROME; NEWBORN; PATHOLOGY; PEDIGREE; RECESSIVE GENE; SYNDROME;

EID: 0036018123     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200207000-00005     Document Type: Article
Times cited : (11)

References (7)
  • 3
    • 0028097370 scopus 로고
    • Aplasia cutis congenita with epibulbar dermoids: Further evidence for syndromic identity of the ocular ectodermal syndrome
    • (1994) Am J Med Genet , vol.53 , pp. 317-320
    • Gardner, J.1    Viljoen, D.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.