SCOPUS 정보 검색 플랫폼

Orbit

Volumn 18, Issue 4, 1999, Pages 247-259

Evaluation of findings in Crouzon's syndrome

(5) Altintas, A G K a Aksoy, F G a Altintas, S C a Midillioglu, I K a Duman, S a

a NONE (Turkey)

Author keywords

Apert syndrome; Congenital malformation; Craniofacial synostosis; Crouzon syndrome; Heredity

Indexed keywords

ACROCEPHALOSYNDACTYLY; ADULT; ARTICLE; CATARACT; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; COMPUTER ASSISTED TOMOGRAPHY; CRANIOFACIAL SYNOSTOSIS; CROUZON SYNDROME; DIFFERENTIAL DIAGNOSIS; DIVERGENT STRABISMUS; EXOPHTHALMOS; FAMILIAL INCIDENCE; FEMALE; HUMAN; HYPERTELORISM; MALE; MAXILLA HYPOPLASIA; MENTAL DEFICIENCY; NOSE MALFORMATION; ORBIT;

EID: 0033333294 PISSN: 01676830 EISSN: None Source Type: Journal
DOI: 10.1076/orbi.18.4.247.2696 Document Type: Article

Times cited : (6)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.