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Volumn 113, Issue 1, 2002, Pages 23-28

Fetal akinesia deformation sequence: A study of 30 consecutive in utero diagnoses

Author keywords

Echography; Fetal akinesia deformation sequence; Fetal pathology; Prenatal diagnosis

Indexed keywords

TERATOGENIC AGENT;

EID: 0037110998     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10698     Document Type: Article
Times cited : (85)

References (21)
  • 1
    • 0027419104 scopus 로고
    • Fatal infantile encephalopathy with olivopontocerebellar hypoplasia and micrencephaly. Report of three siblings
    • Albrecht S, Schneider MC, Belmont J, Armstrong DL. 1993. Fatal infantile encephalopathy with olivopontocerebellar hypoplasia and micrencephaly. Report of three siblings. Acta Neuropathol 85:394-399.
    • (1993) Acta Neuropathol , vol.85 , pp. 394-399
    • Albrecht, S.1    Schneider, M.C.2    Belmont, J.3    Armstrong, D.L.4
  • 7
    • 0031879599 scopus 로고    scopus 로고
    • Marden-Walker syndrome versus isolated distal arthrogryposis: Evidence that both conditions may be variable manifestations of the same mutated gene
    • Fryns JP, Willekens D, Van Schoubroeck D, Moerman P. 1998. Marden-Walker syndrome versus isolated distal arthrogryposis: evidence that both conditions may be variable manifestations of the same mutated gene. Clin Genet 54:86-89.
    • (1998) Clin Genet , vol.54 , pp. 86-89
    • Fryns, J.P.1    Willekens, D.2    Van Schoubroeck, D.3    Moerman, P.4
  • 8
    • 0002253401 scopus 로고
    • Analysis of Pena Shokeir phenotype
    • Hall JG. 1986. Analysis of Pena Shokeir phenotype. Am J Med Genet 25:99-117.
    • (1986) Am J Med Genet , vol.25 , pp. 99-117
    • Hall, J.G.1
  • 9
    • 0020041341 scopus 로고
    • The distal arthrogryposes: Delineation of new entities - Review and nosologic discussion
    • Hall JG, Reed SD, Greene G. 1982a. The distal arthrogryposes: delineation of new entities - review and nosologic discussion. Am J Med Genet 11:185-239.
    • (1982) Am J Med Genet , vol.11 , pp. 185-239
    • Hall, J.G.1    Reed, S.D.2    Greene, G.3
  • 14
    • 0023122838 scopus 로고
    • Olivo-ponto-cerebellar atrophy with muscular atrophy, joint contractures and pulmonary hypoplasia of prenatal onset
    • Moerman P, Barth PG. 1987. Olivo-ponto-cerebellar atrophy with muscular atrophy, joint contractures and pulmonary hypoplasia of prenatal onset. Virchows Arch A Pathol Anat Histopathol 410:339-345.
    • (1987) Virchows Arch A Pathol Anat Histopathol , vol.410 , pp. 339-345
    • Moerman, P.1    Barth, P.G.2
  • 15
    • 0025049703 scopus 로고
    • The fetal akinesia deformation sequence. A fetopathological approach
    • Moerman P, Fryns JP. 1990. The fetal akinesia deformation sequence. A fetopathological approach. Genet Couns 1:25-33.
    • (1990) Genet Couns , vol.1 , pp. 25-33
    • Moerman, P.1    Fryns, J.P.2
  • 16
    • 0011018906 scopus 로고    scopus 로고
    • Acrorenal syndrome in 3 siblings
    • Moerman P, Fryns JP. 1999. Acrorenal syndrome in 3 siblings (abstract). Genet Couns 10:203.
    • (1999) Genet Couns , vol.10 , pp. 203
    • Moerman, P.1    Fryns, J.P.2
  • 18
    • 0026784521 scopus 로고
    • Mucopolysaccharidosis VII as cause of fetal hydrops in early pregnancy
    • Stangenberg M, Lingman G, Roberts G, Ozand P. 1992. Mucopolysaccharidosis VII as cause of fetal hydrops in early pregnancy. Am J Med Genet 44:142-144.
    • (1992) Am J Med Genet , vol.44 , pp. 142-144
    • Stangenberg, M.1    Lingman, G.2    Roberts, G.3    Ozand, P.4
  • 19
    • 0030015386 scopus 로고    scopus 로고
    • Nonimmune hydrops fetalis caused by beta-glucuronidase deficiency (mucopolysaccharidosis VII). Study of a family with 3 affected siblings
    • Van Dorpe J, Moerman P, Pecceu A, Van den SP, Fryns JP. 1996. Nonimmune hydrops fetalis caused by beta-glucuronidase deficiency (mucopolysaccharidosis VII). Study of a family with 3 affected siblings. Genet Couns 7:105-112.
    • (1996) Genet Couns , vol.7 , pp. 105-112
    • Van Dorpe, J.1    Moerman, P.2    Pecceu, A.3    Van den, S.P.4    Fryns, J.P.5
  • 21
    • 0037082978 scopus 로고    scopus 로고
    • Two siblings with early onset fetal akinesia deformation sequence and hydranencephaly: Further evidence for autosomal recessive inheritance of hydranencephaly, Fowler type
    • Witters I, Moerman P, Devriendt K, Braet P, Van Schoubroeck D, Van Assche FA, Fryns JP. 2002. Two siblings with early onset fetal akinesia deformation sequence and hydranencephaly: Further evidence for autosomal recessive inheritance of hydranencephaly, Fowler type. Am J Med Genet 108:41-44.
    • (2002) Am J Med Genet , vol.108 , pp. 41-44
    • Witters, I.1    Moerman, P.2    Devriendt, K.3    Braet, P.4    Van Schoubroeck, D.5    Van Assche, F.A.6    Fryns, J.P.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.