Krawczak M - Search Results

1

Intra- and extragenic marker haplotypes of CFTR mutations in cystic fibrosis families.

Dörk T, Neumann T, Wulbrand U, Wulf B, Kälin N, Maass G, Krawczak M, Guillermit H, Ferec C, Horn G, et al. Dörk T, et al. Among authors: krawczak m. Hum Genet. 1992 Feb;88(4):417-25. doi: 10.1007/BF00215676. Hum Genet. 1992. PMID: 1371263

2

The mutational spectrum of single base-pair substitutions in mRNA splice junctions of human genes: causes and consequences.

Krawczak M, Reiss J, Cooper DN. Krawczak M, et al. Hum Genet. 1992 Sep-Oct;90(1-2):41-54. doi: 10.1007/BF00210743. Hum Genet. 1992. PMID: 1427786

3

Genetic determinants in cystic fibrosis.

Wulbrand U, Dörk T, Tümmler B, Krawczak M. Wulbrand U, et al. Among authors: krawczak m. Lancet. 1991 Mar 9;337(8741):623. doi: 10.1016/0140-6736(91)91697-s. Lancet. 1991. PMID: 1671984 No abstract available.

4

Genotype analysis of cystic fibrosis patients in relation to pancreatic sufficiency.

Stuhrmann M, Macek M Jr, Reis A, Schmidtke J, Tümmler B, Dörk T, Vavrova V, Macek M, Krawczak M. Stuhrmann M, et al. Among authors: krawczak m. Lancet. 1990 Mar 24;335(8691):738-9. doi: 10.1016/0140-6736(90)90862-y. Lancet. 1990. PMID: 1690328 No abstract available.

5

Discrimination between recurrent mutation and identity by descent: application to point mutations in exon 11 of the cystic fibrosis (CFTR) gene.

Reiss J, Cooper DN, Bal J, Slomski R, Cutting GR, Krawczak M. Reiss J, et al. Among authors: krawczak m. Hum Genet. 1991 Aug;87(4):457-61. doi: 10.1007/BF00197168. Hum Genet. 1991. PMID: 1715309

6

Genotype-phenotype correlations in cystic fibrosis patients.

Stuhrmann M, Dörk T, Krawczak M, Dueck M, Banholzer U, Domagk J, Hoffknecht N, Posselt HG, Reis A, Schlösser M, et al. Stuhrmann M, et al. Among authors: krawczak m. Adv Exp Med Biol. 1991;290:97-101; discussion 102-3. doi: 10.1007/978-1-4684-5934-0_12. Adv Exp Med Biol. 1991. PMID: 1719773

7

Frequency of the cystic fibrosis mutation delta F508 in Poland.

Bal J, Maciejko D, Mazurczak T, Potocka A, Krawczak M, Reiss J. Bal J, et al. Among authors: krawczak m. Hum Genet. 1991 Jan;86(3):329. doi: 10.1007/BF00202424. Hum Genet. 1991. PMID: 1997393 No abstract available.

8

Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment.

Krawczak M, Cooper DN. Krawczak M, et al. Hum Genet. 1991 Mar;86(5):425-41. doi: 10.1007/BF00194629. Hum Genet. 1991. PMID: 2016084

9

Frequency of the delta F508 mutation and flanking marker haplotypes at the CF locus from 167 Czech families.

Macek M Jr, Vavrová V, Böhm I, Stuhrmann M, Reis A, Duspivová R, Macek M, Sperling K, Krawczak M, Schmidtke J. Macek M Jr, et al. Among authors: krawczak m. Hum Genet. 1990 Sep;85(4):417-8. doi: 10.1007/BF02428289. Hum Genet. 1990. PMID: 2210755

10

A search for restriction fragment length polymorphism on the human Y chromosome.

Jakubiczka S, Arnemann J, Cooke HJ, Krawczak M, Schmidtke J. Jakubiczka S, et al. Among authors: krawczak m. Hum Genet. 1989 Dec;84(1):86-8. doi: 10.1007/BF00210680. Hum Genet. 1989. PMID: 2575072

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