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Volumn 71, Issue 2, 1997, Pages 150-155

Autosomal dominant microcephaly with normal intelligence, short palpebral fissures, and digital anomalies

Author keywords

Autosomal dominant; Digital anomalies; Microcephaly; Short palpebral fissures; Syndactyly; Thumb hypoplasia

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHILD; CLINICAL ARTICLE; FEMALE; FINGER MALFORMATION; HUMAN; INTELLIGENCE QUOTIENT; MALE; MICROCEPHALY; PALPEBRAL FISSURE ANOMALY; PRIORITY JOURNAL; SYNDACTYLY;

EID: 0030738131     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970808)71:2<150::AID-AJMG6>3.0.CO;2-1     Document Type: Article
Times cited : (13)

References (10)
  • 1
    • 0025797367 scopus 로고
    • Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresia
    • Brunner HG, Winter RM (1991): Autosomal dominant inheritance of abnormalities of the hands and feet with short palpebral fissures, variable microcephaly with learning disability, and oesophageal/duodenal atresia. J Med Genet 28:389-394.
    • (1991) J Med Genet , vol.28 , pp. 389-394
    • Brunner, H.G.1    Winter, R.M.2
  • 2
    • 0003593937 scopus 로고
    • Case report 30
    • Feingold M (1975): Case report 30. Synd Ident 3:16-17.
    • (1975) Synd Ident , vol.3 , pp. 16-17
    • Feingold, M.1
  • 3
    • 0017838162 scopus 로고
    • An unusual microcephaly
    • Feingold M (1978): An unusual microcephaly. Hosp Prac 13:44-49.
    • (1978) Hosp Prac , vol.13 , pp. 44-49
    • Feingold, M.1
  • 5
    • 0002080820 scopus 로고
    • Brain
    • Stevenson RE, Hall JG, Goodman RM (eds): New York: Oxford University Press
    • Hunter A (1993): Brain. In Stevenson RE, Hall JG, Goodman RM (eds): "Human Malformations and Related Anomalies." New York: Oxford University Press, pp 1-19.
    • (1993) Human Malformations and Related Anomalies , pp. 1-19
    • Hunter, A.1
  • 6
    • 0025042565 scopus 로고
    • Microcephaly, mesobrachyphalangy and tracheoesophageal fistula: MMT syndrome
    • König R, Selyer G, Stolp A, Fuchs S (1990): Microcephaly, mesobrachyphalangy and tracheoesophageal fistula: MMT syndrome. Dysmorphol Clin Genet 4:83-86.
    • (1990) Dysmorphol Clin Genet , vol.4 , pp. 83-86
    • König, R.1    Selyer, G.2    Stolp, A.3    Fuchs, S.4
  • 9
    • 0025131567 scopus 로고
    • Microcephaly: General considerations and aids to nosology
    • Opitz JM, Holt MC (1990): Microcephaly: General considerations and aids to nosology. J Craniofac Genet Dev Biol 10:175-204.
    • (1990) J Craniofac Genet Dev Biol , vol.10 , pp. 175-204
    • Opitz, J.M.1    Holt, M.C.2
  • 10
    • 0027500727 scopus 로고
    • Distinctive autosomal or X-linked dominant syndrome of microcephaly, mild developmental delay, short stature, and distinctive face
    • Winter RM (1993): Distinctive autosomal or X-linked dominant syndrome of microcephaly, mild developmental delay, short stature, and distinctive face. Am J Med Genet 47:917-920.
    • (1993) Am J Med Genet , vol.47 , pp. 917-920
    • Winter, R.M.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.