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Volumn 7, Issue 2, 2001, Pages

Trichorhinophalangeal syndrome, type II (Langer-Giedion syndrome)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; CASE REPORT; CHONDRODYSPLASIA; CHROMOSOME 8; CHROMOSOME ANALYSIS; CLUBFOOT; EAR MALFORMATION; EXOSTOSIS; EYEBROW; FEMALE; GROWTH RETARDATION; HUMAN; IRIS COLOBOMA; JAW MALFORMATION; LIP MALFORMATION; MANDIBLE RECONSTRUCTION; METACARPOPHALANGEAL JOINT; MICROGNATHIA; NOSE MALFORMATION; PES EQUINOVARUS; PHILTRUM; PLASTIC SURGERY; PREGNANCY; PTOSIS; RADIODIAGNOSIS; SCANTY HAIR; SHORT STATURE; SUBLUXATION; CLASSIFICATION; CONDUCTION DEAFNESS; DOMINANT GENE; GENETICS; HEREDITARY MULTIPLE EXOSTOSIS; PATHOLOGY;

EID: 0035554501     PISSN: 10872108     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (9)

References (9)
  • 1
    • 0021135775 scopus 로고
    • The tricho-rhinophalangeal syndrome with exostoses (or Langer-Giedion syndrome): Four additional patients without mental retardation and review of the literature
    • Langer LO, Krassikoff N, Laxova R, Scheer-Willaims M, Lutter LD, Gorlin RJ, Jennings CG, Day DW. The tricho-rhinophalangeal syndrome with exostoses (or Langer-Giedion syndrome): four additional patients without mental retardation and review of the literature. Am J Med Genet 1994;19:81-111.
    • (1994) Am J Med Genet , vol.19 , pp. 81-111
    • Langer, L.O.1    Krassikoff, N.2    Laxova, R.3    Scheer-Willaims, M.4    Lutter, L.D.5    Gorlin, R.J.6    Jennings, C.G.7    Day, D.W.8
  • 2
    • 0019455054 scopus 로고
    • Familial tricho-rhino-phalangeal syndrome Type II
    • PubMed
    • Murachi S, Nogami H, Oki T, Ogino T. Familial tricho-rhino-phalangeal syndrome Type II. Clin Genet 1981;19(3):149-55. PubMed
    • (1981) Clin Genet , vol.19 , Issue.3 , pp. 149-155
    • Murachi, S.1    Nogami, H.2    Oki, T.3    Ogino, T.4
  • 3
    • 0021832918 scopus 로고
    • Familial syndrome with some features of the Langer-Giedion syndrome, and paracentric inversion of chromosome 8, inv 8 (q11.23-q21.1)
    • PubMed
    • Shabtai F, Sandowski U, Nissimov R, Klar D, Halbrecht I. Familial syndrome with some features of the Langer-Giedion syndrome, and paracentric inversion of chromosome 8, inv 8 (q11.23-q21.1). Clin Genet 1985;27(6):600-5. PubMed
    • (1985) Clin Genet , vol.27 , Issue.6 , pp. 600-605
    • Shabtai, F.1    Sandowski, U.2    Nissimov, R.3    Klar, D.4    Halbrecht, I.5
  • 4
    • 0026547944 scopus 로고
    • The orthopaedic manifestations of the Langer-Giedion syndrome
    • PubMed
    • Bauermeister S, Letts M. The orthopaedic manifestations of the Langer-Giedion syndrome. Orthop Rev 1992;21(1):31-5. PubMed
    • (1992) Orthop Rev , vol.21 , Issue.1 , pp. 31-35
    • Bauermeister, S.1    Letts, M.2
  • 5
    • 0031592875 scopus 로고    scopus 로고
    • Conductive hearing loss in the tricho-rhino-phalangeal syndrome (TRP II) or in the Langer-Giedion syndrome
    • PubMed
    • Vantrappen G, Feenstra L, Frijns JP. Conductive hearing loss in the tricho-rhino-phalangeal syndrome (TRP II) or in the Langer-Giedion syndrome. Am J Med Genet 1997;72(3):372-3. PubMed
    • (1997) Am J Med Genet , vol.72 , Issue.3 , pp. 372-373
    • Vantrappen, G.1    Feenstra, L.2    Frijns, J.P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.