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Volumn 39, Issue 10, 2002, Pages 714-717

Homozygosity mapping of a Dyggve-Melchior-Clausen syndrome gene to chromosome 18q21.1

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOSAMINOGLYCAN;

EID: 18644368969     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.39.10.714     Document Type: Article
Times cited : (19)

References (15)
  • 1
    • 0000295244 scopus 로고
    • Morquio-Ulrich's disease: An inborn error of metabolism?
    • Dyggve HV, Melchior JC, Clausen J. Morquio-Ulrich's disease: an inborn error of metabolism? Arch Dis Child 1962;37:525-34.
    • (1962) Arch Dis Child , vol.37 , pp. 525-534
    • Dyggve, H.V.1    Melchior, J.C.2    Clausen, J.3
  • 2
    • 0017054955 scopus 로고
    • The Dyggve-Melchior-Clausen syndrome
    • Naffah J. The Dyggve-Melchior-Clausen syndrome. Am J Hum Genet 1976;28:607-14.
    • (1976) Am J Hum Genet , vol.28 , pp. 607-614
    • Naffah, J.1
  • 4
    • 0025338983 scopus 로고
    • Dyggve-Melchior-Clausen syndrome
    • Beighton P. Dyggve-Melchior-Clausen syndrome. J Med Genet 1990;27:512-15.
    • (1990) J Med Genet , vol.27 , pp. 512-515
    • Beighton, P.1
  • 6
    • 0001596256 scopus 로고
    • Sur une forme de dystrophie osseuse famitiale
    • Morquio L. Sur une forme de dystrophie osseuse famitiale. Bull Soc Pediatr 1929;27:145-52.
    • (1929) Bull Soc Pediatr , vol.27 , pp. 145-152
    • Morquio, L.1
  • 9
    • 0021192019 scopus 로고
    • Dyggve-Melchior-Clausen syndrome: Normal degradation of proteodermatan sulfate, proteokeratan sulfate and heparan sulfate
    • Beck M, Lucke R, Kresse H. Dyggve-Melchior-Clausen syndrome: normal degradation of proteodermatan sulfate, proteokeratan sulfate and heparan sulfate. Clin Chim Acta 1983;141:7-15.
    • (1983) Clin Chim Acta , vol.141 , pp. 7-15
    • Beck, M.1    Lucke, R.2    Kresse, H.3
  • 11
    • 0023239442 scopus 로고
    • Homozygosity mapping: A way to map human recessive traits with the DNA of inbred children
    • Lander ES, Botstein D. Homozygosity mapping: a way to map human recessive traits with the DNA of inbred children. Science 1987;236:1567-70.
    • (1987) Science , vol.236 , pp. 1567-1570
    • Lander, E.S.1    Botstein, D.2
  • 12
    • 0021850103 scopus 로고
    • Multilocus linkage analysis in humans: Detection of linkage and estimation of recombination
    • Lathrop GM, Lalouel JM, Julier C, Ott J. Multilocus linkage analysis in humans: detection of linkage and estimation of recombination. Am J Hum Genet 1985;37:482-98.
    • (1985) Am J Hum Genet , vol.37 , pp. 482-498
    • Lathrop, G.M.1    Lalouel, J.M.2    Julier, C.3    Ott, J.4
  • 15
    • 0002663594 scopus 로고
    • Osteochondrodystrophy (Morquio-Brailsford type)
    • Smith R, McCort J. Osteochondrodystrophy (Morquio-Brailsford type). Calif Med 1958;88:55.
    • (1958) Calif Med , vol.88 , pp. 55
    • Smith, R.1    McCort, J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.