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Volumn 8, Issue 4, 1999, Pages 235-240

Expanding the phenotype of Filippi syndrome: A report of three cases

Author keywords

Filippi syndrome; Psychomotor development; Three new patients

Indexed keywords

ARTICLE; CASE REPORT; CHILD; DEVELOPMENTAL DISORDER; FILIPPI SYNDROME; HUMAN; LANGUAGE DISABILITY; MALE; MENTAL RETARDATION MALFORMATION SYNDROME; PHENOTYPE; PRIORITY JOURNAL; SPEECH DISORDER; SYNDROME DELINEATION;

EID: 0032747648     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (10)

References (11)
  • 1
    • 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 22:821-828.
    • (1985) Am J Med Genet , vol.22 , pp. 821-828
    • Filippi, G.1
  • 2
    • 0030021991 scopus 로고    scopus 로고
    • Filippi Syndrome with mild learning difficulties
    • Fryer A (1996). Filippi Syndrome with mild learning difficulties. Clin Dysmorph 5:35-39.
    • (1996) Clin Dysmorph , vol.5 , pp. 35-39
    • Fryer, A.1
  • 5
    • 0025083819 scopus 로고
    • The craniodigital syndrome of Scott: Report of a second family
    • Lorenz P, Hanker GK, Hoffman C, Rupprecht E (1990). The craniodigital syndrome of Scott: Report of a second family. Am J Med Genet 37:224-226.
    • (1990) Am J Med Genet , vol.37 , pp. 224-226
    • Lorenz, P.1    Hanker, G.K.2    Hoffman, C.3    Rupprecht, E.4
  • 6
    • 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 Counselling 4:147-151.
    • (1993) Genet Counselling , vol.4 , pp. 147-151
    • Meinecke, P.1
  • 7
    • 0030867501 scopus 로고    scopus 로고
    • An additional case of craniodigital syndrome: Variable expression of the Filippi syndrome?
    • Orrico A, Hayek G (1997). An additional case of craniodigital syndrome: variable expression of the Filippi syndrome? Clin Genet 52:177-179.
    • (1997) Clin Genet , vol.52 , pp. 177-179
    • Orrico, A.1    Hayek, G.2
  • 8
    • 0023736831 scopus 로고    scopus 로고
    • Sensorineural deafness, hypospadias, and synostosis of metacarpals and metatarsals 4 and 5: A previously apparently undescribed MCA/MR syndrome
    • Pfeiffer RA, Kapfer L (1998). Sensorineural deafness, hypospadias, and synostosis of metacarpals and metatarsals 4 and 5: a previously apparently undescribed MCA/MR syndrome. Am J Med Genet 31:5-10.
    • (1998) Am J Med Genet , vol.31 , pp. 5-10
    • Pfeiffer, R.A.1    Kapfer, L.2
  • 9
    • 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
  • 10
    • 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
  • 11
    • 0026695720 scopus 로고
    • Three sibs with phalangeal anomalies, micro-cephaly, severe mental retardation and neurological abnormalities
    • Woods CG, Crouchman M, Huson SM (1992). Three sibs with phalangeal anomalies, micro-cephaly, 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.