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Volumn 5, Issue 1, 1996, Pages 35-39

Filippi syndrome with mild learning difficulties

Author keywords

Filippi syndrome; Mild developmental delay

Indexed keywords

ARTICLE; CASE REPORT; CHILD; GROWTH RETARDATION; HUMAN; LEARNING DISORDER; MALE; MENTAL DEFICIENCY; MENTAL RETARDATION MALFORMATION SYNDROME; PRIORITY JOURNAL; SIBLING; SYNDACTYLY;

EID: 0030021991     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-199601000-00005     Document Type: Article
Times cited : (12)

References (8)
  • 1
    • 0025834804 scopus 로고
    • New syndrome? Robin sequence with facial and digital anomalies in two half-brothers by the same mother
    • Chitayat D, Meunier CM, Hodgkinson KA, Azouz ME (1991): New syndrome? Robin sequence with facial and digital anomalies in two half-brothers by the same mother. Am J Med Genet 40: 167-172.
    • (1991) Am J Med Genet , vol.40 , pp. 167-172
    • Chitayat, D.1    Meunier, C.M.2    Hodgkinson, K.A.3    Azouz, M.E.4
  • 2
    • 0022369313 scopus 로고
    • Unusual facial appearance, microcephaly, growth and mental retardation and syndactyly. A new syndrome?
    • Filippi G (1985): Unusual facial appearance, microcephaly, growth and mental retardation and syndactyly. A new syndrome? Am J Med Genet 22: 821-824.
    • (1985) Am J Med Genet , vol.22 , pp. 821-824
    • Filippi, G.1
  • 3
    • 0027511392 scopus 로고
    • Microcephaly and digital anomalies: A newly recognised syndrome of recessively inherited mental retardation
    • Kelly TE, Kurson J, Wyatt J (1993): Microcephaly and digital anomalies: a newly recognised 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    Kurson, J.2    Wyatt, J.3
  • 4
    • 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. Genetic Counselling 4: 147-151.
    • (1993) Genetic Counselling , vol.4 , pp. 147-151
    • Meinecke, P.1
  • 5
    • 0015044351 scopus 로고
    • A new craniodigital syndrome with mental retardation
    • Scott CR, Bryant JI, Graham CB (1971): A new craniodigital syndrome with mental retardation. J Pediatr 78: 658-663.
    • (1971) J Pediatr , vol.78 , pp. 658-663
    • Scott, C.R.1    Bryant, J.I.2    Graham, C.B.3
  • 6
    • 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
  • 7
    • 0026695720 scopus 로고
    • Three sibs with phalangeal anomalies, microcephaly, severe mental retardation and neurological abnormalities
    • Woods CG, Crouchman M, Huson SM (1992): Three sibs with phalangeal anomalies, microcephaly, severe mental retardation and neurological abnormalities. J Med Genet 29: 500-502.
    • (1992) J Med Genet , vol.29 , pp. 500-502
    • Woods, C.G.1    Crouchman, M.2    Huson, S.M.3
  • 8
    • 0026573939 scopus 로고
    • Postnatal short stature, microcephaly, severe syndactyly of hands and feet, dysmorphic face and mental retardation: A new syndrome?
    • Zerres K, Rietschel M, Rietschel E, Majewski F, Meinecke P (1992): Postnatal short stature, microcephaly, severe syndactyly of hands and feet, dysmorphic face and mental retardation: a new syndrome? J Med Genet 29: 269-271.
    • (1992) J Med Genet , vol.29 , pp. 269-271
    • Zerres, K.1    Rietschel, M.2    Rietschel, E.3    Majewski, F.4    Meinecke, P.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.