Klasen EC - Search Results

1

Exclusion of the dysplastic nevus syndrome (DNS) locus from the short arm of chromosome 1 by linkage studies in Dutch families.

van Haeringen A, Bergman W, Nelen MR, van der Kooij-Meijs E, Hendrikse I, Wijnen JT, Khan PM, Klasen EC, Frants RR. van Haeringen A, et al. Among authors: klasen ec. Genomics. 1989 Jul;5(1):61-4. doi: 10.1016/0888-7543(89)90086-4. Genomics. 1989. PMID: 2504660

2

Apolipoprotein gene cluster on chromosome 19. Definite localization of the APOC2 gene and the polymorphic Hpa I site associated with type III hyperlipoproteinemia.

Smit M, van der Kooij-Meijs E, Frants RR, Havekes L, Klasen EC. Smit M, et al. Among authors: klasen ec. Hum Genet. 1988 Jan;78(1):90-3. doi: 10.1007/BF00291243. Hum Genet. 1988. PMID: 2892779

3

A Pro----Leu substitution in codon 369 of the alpha-1-antitrypsin deficiency variant PI MHeerlen.

Hofker MH, Nukiwa T, van Paassen HM, Nelen M, Kramps JA, Klasen EC, Frants RR, Crystal RG. Hofker MH, et al. Among authors: klasen ec. Hum Genet. 1989 Feb;81(3):264-8. doi: 10.1007/BF00279001. Hum Genet. 1989. PMID: 2784123

4

Rare apolipoprotein E variant cosegregating with a unique APOE-C1-C2 haplotype in a normolipidemic family.

Smit M, de Knijff P, Sijts A, Klasen EC, Frants RR, Havekes LM. Smit M, et al. Among authors: klasen ec. Hum Hered. 1988;38(5):277-82. doi: 10.1159/000153799. Hum Hered. 1988. PMID: 2906903

5

Cloning and characterization of an alpha 1-antitrypsin like gene 12 KB downstream of the genuine alpha 1-antitrypsin gene.

Hofker MH, Nelen M, Klasen EC, Nukiwa T, Curiel D, Crystal RG, Frants RR. Hofker MH, et al. Among authors: klasen ec. Biochem Biophys Res Commun. 1988 Sep 15;155(2):634-42. doi: 10.1016/s0006-291x(88)80542-4. Biochem Biophys Res Commun. 1988. PMID: 2901833

6

Apolipoprotein E polymorphism in The Netherlands and its effect on plasma lipid and apolipoprotein levels.

Smit M, de Knijff P, Rosseneu M, Bury J, Klasen E, Frants R, Havekes L. Smit M, et al. Hum Genet. 1988 Nov;80(3):287-92. doi: 10.1007/BF01790099. Hum Genet. 1988. PMID: 3192216

7

Familial dysbetalipoproteinemic subjects with the E3/E2 phenotype exhibit an E2 isoform with only one cysteine residue.

Smit M, de Knijff P, Frants RR, Klasen EC, Havekes LM. Smit M, et al. Among authors: klasen ec. Clin Genet. 1987 Nov;32(5):335-41. doi: 10.1111/j.1399-0004.1987.tb03298.x. Clin Genet. 1987. PMID: 3690877

8

Detection of alpha-1-antitrypsin deficiency variants by synthetic oligonucleotide hybridization.

Klasen EC, Hofker MH, van Paassen HM, Verlaan-de Vries M, Bos JL, Frants RR. Klasen EC, et al. Clin Chim Acta. 1987 Dec;170(2-3):201-7. doi: 10.1016/0009-8981(87)90129-x. Clin Chim Acta. 1987. PMID: 3501742

9

The alpha 1 antitrypsin variant PI WFINNEYTOWN in a family of Caucasian origin.

Klasen EC, Laros CD, Bröcker-Vriends A, Frants RR. Klasen EC, et al. Hum Genet. 1985;69(2):190-1. doi: 10.1007/BF00293297. Hum Genet. 1985. PMID: 3871726

10

Linkage studies in facioscapulohumeral muscular dystrophy.

Padberg GW, Klasen EC, Volkers WS, De Lange GG, Wintzen AR. Padberg GW, et al. Among authors: klasen ec. Muscle Nerve. 1988 Aug;11(8):833-5. doi: 10.1002/mus.880110806. Muscle Nerve. 1988. PMID: 3140007

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