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Volumn 51, Issue 3, 1997, Pages 868-872

Improved prenatal diagnosis of the congenital nephrotic syndrome of the Finnish type based on DNA analysis

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 19Q; CLINICAL ARTICLE; DNA DETERMINATION; FETUS; HUMAN; NEPHROTIC SYNDROME; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

EID: 8244242534     PISSN: 00852538     EISSN: None     Source Type: Journal    
DOI: 10.1038/ki.1997.122     Document Type: Article
Times cited : (30)

References (18)
  • 1
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    • Heridity in the congenital nephrotic syndrome: A genetic study of 57 Finnish families with a review of reported cases
    • NORIO R: Heridity in the congenital nephrotic syndrome: A genetic study of 57 Finnish families with a review of reported cases. Ann Peadiatr Fenn 12(Suppl 27):1-94, 1966
    • (1966) Ann Peadiatr Fenn , vol.12 , Issue.27 SUPPL. , pp. 1-94
    • Norio, R.1
  • 2
    • 84981791098 scopus 로고
    • Main features in the congenital nephrotic syndrome
    • HALLMAN N, NORIO R, KOUVALAINEN K: Main features in the congenital nephrotic syndrome. Acta Paediatr Scand 172(Suppl):75-78, 1967
    • (1967) Acta Paediatr Scand , vol.172 , Issue.SUPPL. , pp. 75-78
    • Hallman, N.1    Norio, R.2    Kouvalainen, K.3
  • 3
    • 0017068162 scopus 로고
    • Congenital nephrotic syndrome of Finnish type: Study of 75 patients
    • HUTTUNEN NP: Congenital nephrotic syndrome of Finnish type: Study of 75 patients. Arch Dis Child 51:344-348, 1976
    • (1976) Arch Dis Child , vol.51 , pp. 344-348
    • Huttunen, N.P.1
  • 6
    • 84921013499 scopus 로고
    • Congenital nephrotic syndrome: Prenatal diagnosis and genetic counselling by estimation of amniotic fluid and maternal serum alpha-fetoprotein
    • SEPPÄLÄ M, RAPOLA J, HUTTUNEN N-P, AULA P, KARJALAINEN O, RUOSLAHTI E: Congenital nephrotic syndrome: Prenatal diagnosis and genetic counselling by estimation of amniotic fluid and maternal serum alpha-fetoprotein. Lancet 11:123-124, 1976
    • (1976) Lancet , vol.11 , pp. 123-124
    • Seppälä, M.1    Rapola, J.2    Huttunen, N.-P.3    Aula, P.4    Karjalainen, O.5    Ruoslahti, E.6
  • 9
    • 0039653136 scopus 로고
    • Genetics of congenital and early infantile nephrotic syndrome
    • edited by SPITZER A, AVNER ED, Boston, Dordrecht and London, Kluwer
    • KOSKIMIES O: Genetics of congenital and early infantile nephrotic syndrome, in Inheritage of Kidney and Urinary Tract Diseases, edited by SPITZER A, AVNER ED, Boston, Dordrecht and London, Kluwer, 1990, pp 131-138
    • (1990) Inheritage of Kidney and Urinary Tract Diseases , pp. 131-138
    • Koskimies, O.1
  • 12
    • 0019566438 scopus 로고
    • Renal pathology of fetuses with congenital nephrotic syndrome of the Finnish type: Aqualitative and quantitative electron microscopic study
    • AUTIO-HARMAINEN H: Renal pathology of fetuses with congenital nephrotic syndrome of the Finnish type: Aqualitative and quantitative electron microscopic study. Acta Pathol Microbiol Scand 89:215-222, 1981
    • (1981) Acta Pathol Microbiol Scand , vol.89 , pp. 215-222
    • Autio-Harmainen, H.1
  • 14
    • 0027830447 scopus 로고
    • A single PCR marker in strong allelic association with the infantile form of neuronal ceroid lipofuscionosis facilitates reliable prenatal diagnostics and disease carrier identification
    • VESA J, HELLSTEN E, MÄKELÄ TP, JÄRVELÄ I, AIRAKSINEN T, SANTAVUORI P, PELTONEN L: A single PCR marker in strong allelic association with the infantile form of neuronal ceroid lipofuscionosis facilitates reliable prenatal diagnostics and disease carrier identification. Eur J Hum Genet 1:125-132, 1993
    • (1993) Eur J Hum Genet , vol.1 , pp. 125-132
    • Vesa, J.1    Hellsten, E.2    Mäkelä, T.P.3    Järvelä, I.4    Airaksinen, T.5    Santavuori, P.6    Peltonen, L.7
  • 15
    • 0028936612 scopus 로고
    • Early prenatal diagnosis of cartilage-hair hypolasia (CHH) with polymorphic DNA markers
    • SULISALO T, SILLENCE D, WILSON M, RYYNÄNEN M. KAITILA I: Early prenatal diagnosis of cartilage-hair hypolasia (CHH) with polymorphic DNA markers. Prenatal Diagn 15:135-140, 1995
    • (1995) Prenatal Diagn , vol.15 , pp. 135-140
    • Sulisalo, T.1    Sillence, D.2    Wilson, M.3    Ryynänen, M.4    Kaitila, I.5
  • 16
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    • Haplotype analysis in prenatal diagnosis and carrier identification in Salla disease
    • SCHLEUTKER J, SISTONEN P, AULA P: Haplotype analysis in prenatal diagnosis and carrier identification in Salla disease. (abstract) J Med Genet 33:36, 1995
    • (1995) J Med Genet , vol.33 , pp. 36
    • Schleutker, J.1    Sistonen, P.2    Aula, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.