메뉴 건너뛰기




Volumn 15, Issue 3, 1977, Pages 301-309

Craniosynostosis. II. Coronal synostosis: Its familial characteristics and associated clinical findings in 109 patients lacking bilateral polysyndactyly or syndactyly

Author keywords

[No Author keywords available]

Indexed keywords

CONGENITAL HEART MALFORMATION; CORONAL SUTURE; CRANIOFACIAL SYNOSTOSIS; DIAGNOSIS; ETIOLOGY; MAJOR CLINICAL STUDY; MENTAL DEFICIENCY; PEDIGREE; RECURRENCE RISK; SYNOSTOSIS; ARTICLE; CLEFT PALATE; CONGENITAL MALFORMATION; FEMALE; FINGER; GENETICS; HUMAN; MALE; MULTIPLE MALFORMATION SYNDROME; PATHOLOGY; SEX DIFFERENCE; TOE;

EID: 0017623193     PISSN: 00403709     EISSN: 10969926     Source Type: Journal    
DOI: 10.1002/tera.1420150312     Document Type: Article
Times cited : (81)

References (19)
  • 4
    • 72849168864 scopus 로고
    • Apert's syndrome (a type of acrocephaloayndactyly): Observations on a British series of thirty‐nine cases
    • (1960) Ann. Hum. Genet. , vol.24 , pp. 151-164
    • Blank, C.E.1
  • 9
    • 84989016011 scopus 로고
    • The Natural history of aminopterin induced embryopathy. Birth Defects: Original Article Series 1976 Birth Defects Conference, in press.
    • (1976)
    • Howard, N.J.1    Rudd, N.L.2
  • 12
    • 0017009226 scopus 로고
    • Craniosynostosis. I: Coronal synostosis; its genetic and associated clinical findings in 214 patients who lacked involvement of the coronal suture(s)
    • (1976) Teratology , vol.14 , pp. 185-194
    • Hunter, A.G.W.1    Rudd, N.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.