메뉴 건너뛰기




Volumn 69, Issue 3, 1997, Pages 240-244

Digital anomalies, microcephaly, and normal intelligence: New syndrome or Feingold syndrome?

Author keywords

brachydactyly; digital abnormalities; microcephaly; syndactyly

Indexed keywords

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BRACHYDACTYLY; CASE REPORT; CLINODACTYLY; FEMALE; FINGER MALFORMATION; GENETIC COUNSELING; HUMAN; INTELLIGENCE; MALE; MICROCEPHALY; PRESCHOOL CHILD; PRIORITY JOURNAL; SYNDACTYLY; SYNDROME;

EID: 0030959498     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19970331)69:3<240::AID-AJMG6>3.0.CO;2-P     Document Type: Article
Times cited : (8)

References (13)
  • 1
    • 0002070475 scopus 로고
    • On brachydactyly and symphalangism
    • Bell J (1951): On brachydactyly and symphalangism. Treasury Hum Inherit 5:1-30.
    • (1951) Treasury Hum Inherit , vol.5 , pp. 1-30
    • Bell, J.1
  • 2
    • 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
  • 3
    • 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
  • 4
    • 0017838162 scopus 로고
    • An unusual microcephaly
    • Feingold M (1978): An unusual microcephaly. Hosp Pract 13:44, 49.
    • (1978) Hosp Pract , vol.13 , pp. 44
    • Feingold, M.1
  • 5
    • 0022369313 scopus 로고
    • Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly
    • Filippi G (1985): Unusual facial appearance, microcephaly, growth and mental retardation, and syndactyly. A new syndrome? Am J Med Genet 22:821-824.
    • (1985) A New Syndrome? Am J Med Genet , vol.22 , pp. 821-824
    • Filippi, G.1
  • 6
    • 0018409706 scopus 로고
    • Classification and identification of inherited brachydactylies
    • Fitch N (1979): Classification and identification of inherited brachydactylies. J Med Genet 16:36-44.
    • (1979) J Med Genet , vol.16 , pp. 36-44
    • Fitch, N.1
  • 7
    • 0027511392 scopus 로고
    • Microcephaly and digital anomalies: A newly recognized syndrome of recessively inherited mental retardation
    • Kelly TE, Kirson L, Wyatt J (1993): Microcephaly and digital anomalies: A newly recognized syndrome of recessively inherited mental retardation. Am J Med Genet 45:353-355.
    • (1993) Am J Med Genet , vol.45 , pp. 353-355
    • Kelly, T.E.1    Kirson, L.2    Wyatt, J.3
  • 8
    • 0025042565 scopus 로고
    • Microcephaly, mesobrachyphalangy, and tracheoesophagcal fistula: MMT syndrome
    • Konig R, Selzer G, Stolp A, Fuchs S (1990): Microcephaly, mesobrachyphalangy, and tracheoesophagcal fistula: MMT syndrome. Dysmorphol Clini Genet 4:83-86.
    • (1990) Dysmorphol Clini Genet , vol.4 , pp. 83-86
    • Konig, R.1    Selzer, G.2    Stolp, A.3    Fuchs, S.4
  • 9
    • 0027207605 scopus 로고
    • Short stature, microcephaly, characteristic face, syndactyly and mental retardation: The Filippi syndrome report on a second family
    • Meinecke P (1993): Short stature, microcephaly, characteristic face, syndactyly and mental retardation: The Filippi syndrome report on a second family. Genet Counseling 4:147-151.
    • (1993) Genet Counseling , vol.4 , pp. 147-151
    • Meinecke, P.1
  • 10
    • 0025131567 scopus 로고
    • Microcephaly: General considerations and aids to nosology
    • Opitz JM, Holt MC (1990): Microcephaly: General considerations and aids to nosology. J Craniofacial Genet Dev Biol 10:175-204.
    • (1990) J Craniofacial Genet Dev Biol , vol.10 , pp. 175-204
    • Opitz, J.M.1    Holt, M.C.2
  • 11
    • 0013656160 scopus 로고
    • The genetics of hand malformations
    • Temtamy SA, McKusick VA (1978): The genetics of hand malformations. Birth Defects 14:1-619.
    • (1978) Birth Defects , vol.14 , pp. 1-619
    • Temtamy, S.A.1    McKusick, V.A.2
  • 12
    • 0028897567 scopus 로고
    • Craniodigital syndromes: Report of a child with Filippi syndrome and discussion of differential diagnosis
    • Toriello HV, Higgins JV (1995): Craniodigital syndromes: Report of a child with Filippi syndrome and discussion of differential diagnosis. Am J Med Genet 55:200-204.
    • (1995) Am J Med Genet , vol.55 , pp. 200-204
    • Toriello, H.V.1    Higgins, J.V.2
  • 13
    • 0342862559 scopus 로고
    • Hands and feet
    • Stevenson RE, Hall. JG. Goodman RM (eds): Oxford: Oxford University Press
    • Winter RM, Schroer RJ, Meyer LC (1993): Hands and feet. In Stevenson RE, Hall. JG. Goodman RM (eds): "Human Malformations and Related Anomalies," Vol. II. Oxford: Oxford University Press, pp 805-843.
    • (1993) Human Malformations and Related Anomalies , vol.2 , pp. 805-843
    • Winter, R.M.1    Schroer, R.J.2    Meyer, L.C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.