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Volumn 8, Issue 10, 1997, Pages 783-784

An assay for the Cpefat obesity mutation created with a modified primer

Author keywords

[No Author keywords available]

Indexed keywords

CARBOXYPEPTIDASE; CARBOXYPEPTIDASE H; DNA; PRIMER DNA; TYPE II SITE SPECIFIC DEOXYRIBONUCLEASE;

EID: 0030611180     PISSN: 09388990     EISSN: None     Source Type: Journal    
DOI: 10.1007/s003359900568     Document Type: Article
Times cited : (5)

References (6)
  • 1
    • 0025627770 scopus 로고
    • Fat (fat) and Tubby (tub): Two autosomal recessive mutations causing obesity syndromes in the mouse
    • Coleman DL, Eicher EM (1990) Fat (fat) and Tubby (tub): two autosomal recessive mutations causing obesity syndromes in the mouse. J Hered 81, 424-427
    • (1990) J Hered , vol.81 , pp. 424-427
    • Coleman, D.L.1    Eicher, E.M.2
  • 2
    • 0025752980 scopus 로고
    • Application of natural and amplification created restriction sites for the diagnosis of PKU mutations
    • Eiken HG, Odlund E, Boman H, Skjelkvåle L, Engebretsen LF, Apold J (1991) Application of natural and amplification created restriction sites for the diagnosis of PKU mutations. Nucleic Acids Res 19, 1427-1430
    • (1991) Nucleic Acids Res , vol.19 , pp. 1427-1430
    • Eiken, H.G.1    Odlund, E.2    Boman, H.3    Skjelkvåle, L.4    Engebretsen, L.F.5    Apold, J.6
  • 3
    • 0028922293 scopus 로고
    • Multiplex genotype determination at a DNA sequence polymorphism in the human immunoglobulin heavy-chain region
    • Li H, Hood L (1995) Multiplex genotype determination at a DNA sequence polymorphism in the human immunoglobulin heavy-chain region. Genomics 26, 199-206
    • (1995) Genomics , vol.26 , pp. 199-206
    • Li, H.1    Hood, L.2
  • 5
    • 0025754172 scopus 로고
    • Diagnosis of genetic disease by primerspecified restriction map modification, with application to cystic fibrosis and retinitis pigmentosa
    • Sorscher EJ, Huang Z (1991) Diagnosis of genetic disease by primerspecified restriction map modification, with application to cystic fibrosis and retinitis pigmentosa. Lancet 337, 1115-1118
    • (1991) Lancet , vol.337 , pp. 1115-1118
    • Sorscher, E.J.1    Huang, Z.2
  • 6
    • 0026342119 scopus 로고
    • Hereditary hydronephrosis in C57BL/KSJ mice
    • Weide LG, Lacy PE (1991) Hereditary hydronephrosis in C57BL/KSJ mice. Lab Anim Sci 41, 415-418
    • (1991) Lab Anim Sci , vol.41 , pp. 415-418
    • Weide, L.G.1    Lacy, P.E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.