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Volumn 41, Issue 1, 2008, Pages 76-78

Radial, renal and craniofacial anomalies: Baller-Gerold syndrome

Author keywords

Baller Gerold syndrome; Craniosynostosis; Crossed ectopia; Ectopic kidneys; Microcephaly; Radial agenesis; Radial club hand; Reflux; Renal agenesis; Vesico ureteric reflux

Indexed keywords


EID: 45549105673     PISSN: 09700358     EISSN: 1998376X     Source Type: Journal    
DOI: 10.4103/0970-0358.41118     Document Type: Article
Times cited : (2)

References (14)
  • 2
    • 0000042326 scopus 로고
    • Healing of a fracture in an unusual case of congenital anomaly of the upper extremities
    • Gerold M. Healing of a fracture in an unusual case of congenital anomaly of the upper extremities. Zbl Chir 1959;84:831-4.
    • (1959) Zbl Chir , vol.84 , pp. 831-834
    • Gerold, M.1
  • 4
    • 0028244052 scopus 로고
    • Phenotypic variability in the Baller-Gerold syndrome: Report of a mildly affected patient and review of the literature
    • Ramos Fuentes FJ, Nicholson L, Scott CI Jr. Phenotypic variability in the Baller-Gerold syndrome: Report of a mildly affected patient and review of the literature. Eur J Pediatr 1994;153:483-7.
    • (1994) Eur J Pediatr , vol.153 , pp. 483-487
    • Ramos Fuentes, F.J.1    Nicholson, L.2    Scott Jr., C.I.3
  • 5
    • 0016722568 scopus 로고
    • An etiologic and nosologic overview of craniosynostosis syndromes
    • Cohen MM Jr. An etiologic and nosologic overview of craniosynostosis syndromes. Birth Defects 1975;11:137-89.
    • (1975) Birth Defects , vol.11 , pp. 137-189
    • Cohen Jr., M.M.1
  • 9
    • 0033555855 scopus 로고    scopus 로고
    • TWIST gene mutation in a patient with radial aplasia and craniosynostosis: Further evidence for heterogeneity of Baller-Gerold syndrome
    • Gripp KW, Stolle CA, Celle L, McDonald-McGinn DM, Whitaker LA, Zackai EH. TWIST gene mutation in a patient with radial aplasia and craniosynostosis: Further evidence for heterogeneity of Baller-Gerold syndrome. Am J Med Genet 1999;82:170-6.
    • (1999) Am J Med Genet , vol.82 , pp. 170-176
    • Gripp, K.W.1    Stolle, C.A.2    Celle, L.3    McDonald-McGinn, D.M.4    Whitaker, L.A.5    Zackai, E.H.6
  • 10
    • 0141756130 scopus 로고    scopus 로고
    • Expanding the phenotypic spectrum of the Baller-Gerold syndrome
    • Temtamy SA, Aglan MS, Nemat A, Eid M. Expanding the phenotypic spectrum of the Baller-Gerold syndrome. Genet Couns 2003;14:299-312.
    • (2003) Genet Couns , vol.14 , pp. 299-312
    • Temtamy, S.A.1    Aglan, M.S.2    Nemat, A.3    Eid, M.4
  • 12
    • 0025289046 scopus 로고
    • The Baller-Gerold syndrome: Phenotypic and cytogenetic overlap with Roberts syndrome
    • Huson SM, Rodgers CS, Hall CM, Winter RM. The Baller-Gerold syndrome: Phenotypic and cytogenetic overlap with Roberts syndrome. J Med Genet 1990;27:371-5.
    • (1990) J Med Genet , vol.27 , pp. 371-375
    • Huson, S.M.1    Rodgers, C.S.2    Hall, C.M.3    Winter, R.M.4
  • 13
    • 0028265083 scopus 로고
    • Fanconi anemia in a child previously diagnosed as Baller-Gerold syndrome
    • Farrell SA, Paes BA, Lewis ME. Fanconi anemia in a child previously diagnosed as Baller-Gerold syndrome. Am J Med Genet 1994;50:98-9.
    • (1994) Am J Med Genet , vol.50 , pp. 98-99
    • Farrell, S.A.1    Paes, B.A.2    Lewis, M.E.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.