Kere J - Search Results

1

Fine mapping of the congenital chloride diarrhea gene by linkage disequilibrium.

Höglund P, Sistonen P, Norio R, Holmberg C, Dimberg A, Gustavson KH, de la Chapelle A, Kere J. Höglund P, et al. Among authors: kere j. Am J Hum Genet. 1995 Jul;57(1):95-102. Am J Hum Genet. 1995. PMID: 7611301 Free PMC article.

2

Familial amyloidosis, Finnish type: G654----a mutation of the gelsolin gene in Finnish families and an unrelated American family.

de la Chapelle A, Kere J, Sack GH Jr, Tolvanen R, Maury CP. de la Chapelle A, et al. Among authors: kere j. Genomics. 1992 Jul;13(3):898-901. doi: 10.1016/0888-7543(92)90182-r. Genomics. 1992. PMID: 1322359

3

Homozygosity for the Asn187 gelsolin mutation in Finnish-type familial amyloidosis is associated with severe renal disease.

Maury CP, Kere J, Tolvanen R, de la Chapelle A. Maury CP, et al. Among authors: kere j. Genomics. 1992 Jul;13(3):902-3. doi: 10.1016/0888-7543(92)90183-s. Genomics. 1992. PMID: 1322360 No abstract available.

4

Gelsolin-derived familial amyloidosis caused by asparagine or tyrosine substitution for aspartic acid at residue 187.

de la Chapelle A, Tolvanen R, Boysen G, Santavy J, Bleeker-Wagemakers L, Maury CP, Kere J. de la Chapelle A, et al. Among authors: kere j. Nat Genet. 1992 Oct;2(2):157-60. doi: 10.1038/ng1092-157. Nat Genet. 1992. PMID: 1338910

5

[The gene defect for Finnish hereditary amyloidosis has been found].

Maury CP, Kere J, Baumann M, de la Chapelle A. Maury CP, et al. Among authors: kere j. Duodecim. 1991;107(16):1344-5. Duodecim. 1991. PMID: 1365358 Review. Finnish. No abstract available.

6

Evidence that the MCC-APC gene region in 5q21 is not the site for susceptibility to hereditary nonpolyposis colorectal carcinoma.

Peltomäki P, Sistonen P, Mecklin JP, Pylkkänen L, Aaltonen L, Nordling S, Kere J, Järvinen H, Hamilton SR, Petersen G, et al. Peltomäki P, et al. Among authors: kere j. Cancer Res. 1992 Aug 15;52(16):4530-3. Cancer Res. 1992. PMID: 1643645

7

Refinement of human chromosome 7 map around the pro alpha 2(I)collagen gene by long-range restriction mapping.

Kere J, Tolvanen R, Donis-Keller H, de la Chapelle A. Kere J, et al. Nucleic Acids Res. 1991 May 25;19(10):2755-9. doi: 10.1093/nar/19.10.2755. Nucleic Acids Res. 1991. PMID: 2041749 Free PMC article.

8

Finnish hereditary amyloidosis is caused by a single nucleotide substitution in the gelsolin gene.

Maury CP, Kere J, Tolvanen R, de la Chapelle A. Maury CP, et al. Among authors: kere j. FEBS Lett. 1990 Dec 10;276(1-2):75-7. doi: 10.1016/0014-5793(90)80510-p. FEBS Lett. 1990. PMID: 2176164 Free article.

9

Cystic fibrosis mutation delta F508 in Finland: other mutations predominate.

Kere J, Savilahti E, Norio R, Estivill X, de la Chapelle A. Kere J, et al. Hum Genet. 1990 Sep;85(4):413-5. doi: 10.1007/BF02428286. Hum Genet. 1990. PMID: 2210753

10

Chromosome 7 long arm deletion in myeloid disorders: a narrow breakpoint region in 7q22 defined by molecular mapping.

Kere J, Ruutu T, Davies KA, Roninson IB, Watkins PC, Winqvist R, de la Chapelle A. Kere J, et al. Blood. 1989 Jan;73(1):230-4. Blood. 1989. PMID: 2562922 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

615 results

Search Page

Filters