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Volumn 61, Issue 2, 1996, Pages 174-177

Craniosynostosis, microcephaly, hydrancephaly, humero-radial synostosis, and thumb aplasia: A new syndrome?

Author keywords

craniosynostosis; humeroradial synostosis; hydrancephaly; microcephaly; thumb aplasia

Indexed keywords

APLASIA; ARTICLE; CASE REPORT; CRANIOFACIAL SYNOSTOSIS; GROWTH RETARDATION; HUMAN; INFANT; MALE; MALFORMATION SYNDROME; MICROCEPHALY; PRIORITY JOURNAL; SYNOSTOSIS; THUMB MALFORMATION;

EID: 0030058202     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19960111)61:2<174::AID-AJMG15>3.0.CO;2-R     Document Type: Article
Times cited : (4)

References (13)
  • 1
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    • (1985) Am J Med Genet , vol.20 , pp. 203-204
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  • 2
    • 0015176564 scopus 로고
    • The adducted thumbs syndrome: An autosomal recessive disease with arthrogryposis, dysmyelination, craniostenosis, and cleft palate
    • Christian JC, Andrews PA, Conneally PM, Muller J (1971): The adducted thumbs syndrome: An autosomal recessive disease with arthrogryposis, dysmyelination, craniostenosis, and cleft palate. Clin Genet 2:95-103.
    • (1971) Clin Genet , vol.2 , pp. 95-103
    • Christian, J.C.1    Andrews, P.A.2    Conneally, P.M.3    Muller, J.4
  • 6
    • 0025289046 scopus 로고
    • The Baller-Gerold syndrome: Phenotypic and cytogenetic overlap with Roberts syndrome
    • Huson SM, Rogers CS, Hall CM, Winter RM (1990): The Baller-Gerold syndrome: Phenotypic and cytogenetic overlap with Roberts syndrome. J Med Genet 27:371-375.
    • (1990) J Med Genet , vol.27 , pp. 371-375
    • Huson, S.M.1    Rogers, C.S.2    Hall, C.M.3    Winter, R.M.4
  • 7
    • 0026000151 scopus 로고
    • Radial ray defects, triangular face, telecanthus, sparse hair, dwarfism and mental retardation
    • Imaizumi K, Kuroki Y (1991): Radial ray defects, triangular face, telecanthus, sparse hair, dwarfism and mental retardation. Am J Med Genet 41:162-163.
    • (1991) Am J Med Genet , vol.41 , pp. 162-163
    • Imaizumi, K.1    Kuroki, Y.2
  • 8
    • 0019176298 scopus 로고
    • Autosomal recessive microcephaly and micromelia in Cree Indians
    • Ives EJ, Houston CJ (1980): Autosomal recessive microcephaly and micromelia in Cree Indians. Am J Med Genet 7:351-360.
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    • Ives, E.J.1    Houston, C.J.2
  • 9
    • 0027468193 scopus 로고
    • New syndrome with features overlapping the Baller-Gerold and Roberts syndromes
    • Newbury-Ecob RA, McKeever PA, Gosden C, Young ID (1993): New syndrome with features overlapping the Baller-Gerold and Roberts syndromes. Clin Dysmorph 2:173-177.
    • (1993) Clin Dysmorph , vol.2 , pp. 173-177
    • Newbury-Ecob, R.A.1    McKeever, P.A.2    Gosden, C.3    Young, I.D.4
  • 10
    • 0023155838 scopus 로고
    • Sagittal craniostenosis, congenital heart disease, mental deficiency, and various dysmorphies in two sibs - A "new" syndrome
    • Pfeiffer RA, Singer H, Zschiesche S (1987): Sagittal craniostenosis, congenital heart disease, mental deficiency, and various dysmorphies in two sibs - a "new" syndrome. Eur J Pediatr 146:75-78.
    • (1987) Eur J Pediatr , vol.146 , pp. 75-78
    • Pfeiffer, R.A.1    Singer, H.2    Zschiesche, S.3
  • 13
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    • Craniosynostosis with associated cranial base anomalies: A morphologic and histologic study of affected like-sexed twins
    • Woon K-C, Kokich VG, Clarren SK, Cohen MM Jr (1980): Craniosynostosis with associated cranial base anomalies: A morphologic and histologic study of affected like-sexed twins. Teratology 22:23-35.
    • (1980) Teratology , vol.22 , pp. 23-35
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.