-
1
-
-
0038424730
-
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
-
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
-
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
-
4
-
-
0026079277
-
Renal transplantation in small children with congenital nephrotic syndrome of the Finnish type
-
HOLMBERG C, JALANKO H, KOSKIMIES O, LEIJALA M, SALMELA K, EKLUND B, AHONEN J: Renal transplantation in small children with congenital nephrotic syndrome of the Finnish type. Transplant Proc 23:1378-1379, 1991
-
(1991)
Transplant Proc
, vol.23
, pp. 1378-1379
-
-
Holmberg, C.1
Jalanko, H.2
Koskimies, O.3
Leijala, M.4
Salmela, K.5
Eklund, B.6
Ahonen, J.7
-
5
-
-
0028842315
-
Management of congenital nephrotic syndrome of the Finnish type
-
HOLMBERG C, ANTIKAINEN M, RÖNNHOLM K, ALA-HOUHALA M, JALANKO H: Management of congenital nephrotic syndrome of the Finnish type. Pediatr Nephrol 9:87-93, 1995
-
(1995)
Pediatr Nephrol
, vol.9
, pp. 87-93
-
-
Holmberg, C.1
Antikainen, M.2
Rönnholm, K.3
Ala-Houhala, M.4
Jalanko, H.5
-
6
-
-
84921013499
-
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
-
7
-
-
0028329864
-
Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19
-
KESTILÄ M, MÄNNIKKÖ M, HOLMBERG C, GYAPAY G, WEISSENBACH J, SAVOLAINEN ER, PELTONEN L: Congenital nephrotic syndrome of the Finnish type maps to the long arm of chromosome 19. Am J Hum Genet 54:757-764, 1994
-
(1994)
Am J Hum Genet
, vol.54
, pp. 757-764
-
-
Kestilä, M.1
Männikkö, M.2
Holmberg, C.3
Gyapay, G.4
Weissenbach, J.5
Savolainen, E.R.6
Peltonen, L.7
-
8
-
-
0028863565
-
Fine mapping and haplotype analysis of the locus for congenital nephrotic syndrome on chromosome 19q13.1
-
MÄNNIKKÖ M, KESTILÄ M, HOLMBERG R, NORIO R, RYYNÄNEN M, OLSEN A, PELTONEN L, TRYGGVASON K: Fine mapping and haplotype analysis of the locus for congenital nephrotic syndrome on chromosome 19q13.1. Am J Hum Genet 57:1377-1383, 1995
-
(1995)
Am J Hum Genet
, vol.57
, pp. 1377-1383
-
-
Männikkö, M.1
Kestilä, M.2
Holmberg, R.3
Norio, R.4
Ryynänen, M.5
Olsen, A.6
Peltonen, L.7
Tryggvason, K.8
-
9
-
-
0039653136
-
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
-
10
-
-
0003968221
-
-
Oxford, Washington DC, IRL Press
-
DAVIES KE: Human Genetic Diseases, A Practical Approach. Oxford, Washington DC, IRL Press, 1986, pp 1-5
-
(1986)
Human Genetic Diseases, A Practical Approach
, pp. 1-5
-
-
Davies, K.E.1
-
11
-
-
0342499587
-
Strategies for multilocus linkage analysis in humans
-
LATHROP GM, LALOUEL JM, JULIER C, OTT J: Strategies for multilocus linkage analysis in humans. Proc Natl Acad Sci USA 81:3443-3446, 1984
-
(1984)
Proc Natl Acad Sci USA
, vol.81
, pp. 3443-3446
-
-
Lathrop, G.M.1
Lalouel, J.M.2
Julier, C.3
Ott, J.4
-
12
-
-
0019566438
-
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
-
13
-
-
0027402012
-
Prenatal diagnosis of diastrophic dysplasia with polymorphic DNA markers
-
HÄSTBACKA J, SALONEN R, LAURILA P, DE LA CHAPELLE A, KAITILA I: Prenatal diagnosis of diastrophic dysplasia with polymorphic DNA markers. J Med Genet 30:265-268, 1993
-
(1993)
J Med Genet
, vol.30
, pp. 265-268
-
-
Hästbacka, J.1
Salonen, R.2
Laurila, P.3
De La Chapelle, A.4
Kaitila, I.5
-
14
-
-
0027830447
-
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
-
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
-
-
0030049540
-
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
-
17
-
-
0027365391
-
Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat polymorphism linkage map of chromosome 19
-
WEBER JL, WANG Z, HANSEN K, STEPHENSON M, KAPPEL C, SALZMAN S, WILKIE PJ, KEATS B:1079-1095 Dracopoli NC, Brandriff BF, Olsen AS: Evidence for human meiotic recombination interference obtained through construction of a short tandem repeat polymorphism linkage map of chromosome 19. Am J Hum Genet 53:1993
-
(1993)
Am J Hum Genet
, vol.53
-
-
Weber, J.L.1
Wang, Z.2
Hansen, K.3
Stephenson, M.4
Kappel, C.5
Salzman, S.6
Wilkie, P.J.7
Keats, B.8
Dracopoli, N.C.9
Brandriff, B.F.10
Olsen, A.S.11
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