Kere J - Search Results

1

Assignment of a novel locus for autosomal recessive congenital ichthyosis to chromosome 19p13.1-p13.2.

Virolainen E, Wessman M, Hovatta I, Niemi KM, Ignatius J, Kere J, Peltonen L, Palotie A. Virolainen E, et al. Among authors: kere j. Am J Hum Genet. 2000 Mar;66(3):1132-7. doi: 10.1086/302813. Am J Hum Genet. 2000. PMID: 10712223 Free PMC article.

2

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

3

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

4

Cystic fibrosis in Finland: a molecular and genealogical study.

Kere J, Norio R, Savilahti E, Estivill X, de la Chapelle A. Kere J, et al. Hum Genet. 1989 Aug;83(1):20-5. doi: 10.1007/BF00274141. Hum Genet. 1989. PMID: 2570015

5

Cystic fibrosis in a low-incidence population: two major mutations in Finland.

Kere J, Estivill X, Chillón M, Morral N, Nunes V, Norio R, Savilahti E, de la Chapelle A. Kere J, et al. Hum Genet. 1994 Feb;93(2):162-6. doi: 10.1007/BF00210603. Hum Genet. 1994. PMID: 7509311

6

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.

7

Paternal isodisomy for chromosome 7 is compatible with normal growth and development in a patient with congenital chloride diarrhea.

Höglund P, Holmberg C, de la Chapelle A, Kere J. Höglund P, et al. Among authors: kere j. Am J Hum Genet. 1994 Oct;55(4):747-52. Am J Hum Genet. 1994. PMID: 7942853 Free PMC article.

8

A rare reciprocal translocation (12;21) segregating for nine generations.

Koskinen S, Onnelainen T, de la Chapelle A, Kere J. Koskinen S, et al. Among authors: kere j. Hum Genet. 1993 Nov;92(5):509-12. doi: 10.1007/BF00216460. Hum Genet. 1993. PMID: 8244343 Review.

9

Split hand/split foot malformation, deafness, and mental retardation with a complex cytogenetic rearrangement involving 7q21.3.

Ignatius J, Knuutila S, Scherer SW, Trask B, Kere J. Ignatius J, et al. Among authors: kere j. J Med Genet. 1996 Jun;33(6):507-10. doi: 10.1136/jmg.33.6.507. J Med Genet. 1996. PMID: 8782053 Free PMC article.

10

Anhidrotic ectodermal dysplasia (EDA) protein expressed in MCF-7 cells associates with cell membrane and induces rounding.

Ezer S, Schlessinger D, Srivastava A, Kere J. Ezer S, et al. Among authors: kere j. Hum Mol Genet. 1997 Sep;6(9):1581-7. doi: 10.1093/hmg/6.9.1581. Hum Mol Genet. 1997. PMID: 9285797

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