Kähkönen M - Search Results

1

Comparative genomic hybridization studies in tumours from a patient with multiple endocrine neoplasia type 1.

Kytölä S, Mäkinen MJ, Kähkönen M, Teh BT, Leisti J, Salmela P. Kytölä S, et al. Among authors: kahkonen m. Eur J Endocrinol. 1998 Aug;139(2):202-6. doi: 10.1530/eje.0.1390202. Eur J Endocrinol. 1998. PMID: 9724078

2

A molecular and cytogenetic study in Finnish Prader-Willi patients.

Kokkonen H, Kähkönen M, Leisti J. Kokkonen H, et al. Among authors: kahkonen m. Hum Genet. 1995 May;95(5):568-71. doi: 10.1007/BF00223871. Hum Genet. 1995. PMID: 7759080

3

Diagnosis of fragile X syndrome by direct mutation analysis.

Väisänen ML, Kähkönen M, Leisti J. Väisänen ML, et al. Among authors: kahkonen m. Hum Genet. 1994 Feb;93(2):143-7. doi: 10.1007/BF00210599. Hum Genet. 1994. PMID: 8112737

4

Carrier detection of the fragile X syndrome with flanking RFLP markers and linkage analysis.

Väisänen ML, Kähkönen M, Leisti J. Väisänen ML, et al. Among authors: kahkonen m. Am J Med Genet. 1992 Apr 15-May 1;43(1-2):307-11. doi: 10.1002/ajmg.1320430147. Am J Med Genet. 1992. PMID: 1351364

5

Uridine enhances expression of the fragile X chromosome in human lymphocytes.

Kähkönen M, Haataja R, Leisti J. Kähkönen M, et al. Hum Genet. 1991 May;87(1):95-6. doi: 10.1007/BF01213102. Hum Genet. 1991. PMID: 2037287

6

A patient with Wolf-Hirschhorn syndrome originating from translocation t(4;8) (p16.3;q24.3)pat.

el-Rifai W, Leisti J, Kähkönen M, Pietarinen A, Altherr MR, Knuutila S. el-Rifai W, et al. Among authors: kahkonen m. J Med Genet. 1995 Jan;32(1):65-7. doi: 10.1136/jmg.32.1.65. J Med Genet. 1995. PMID: 7897631 Free PMC article.

7

Prenatal diagnosis of single gene disorders in northern Finland.

Leisti J, Jouppila P, Mustonen A, Kähkönen M, Herva R, Ruokonen A, Kirkinen P. Leisti J, et al. Among authors: kahkonen m. Ann Med. 1990 Apr;22(2):123-9. doi: 10.3109/07853899009147254. Ann Med. 1990. PMID: 2193659 Free article.

8

A new RFLP with StuI and probe cX55.7 (DXS105) and its usefulness in carrier analysis of fragile X syndrome.

Rekilä AM, Väisänen ML, Kähkönen M, Leisti J, Winqvist R. Rekilä AM, et al. Among authors: kahkonen m. Hum Genet. 1988 Oct;80(2):193. doi: 10.1007/BF00702869. Hum Genet. 1988. PMID: 2902001

9

Primary cutaneous T-cell lymphomas show a deletion or translocation affecting NAV3, the human UNC-53 homologue.

Karenko L, Hahtola S, Päivinen S, Karhu R, Syrjä S, Kähkönen M, Nedoszytko B, Kytölä S, Zhou Y, Blazevic V, Pesonen M, Nevala H, Nupponen N, Sihto H, Krebs I, Poustka A, Roszkiewicz J, Saksela K, Peterson P, Visakorpi T, Ranki A. Karenko L, et al. Among authors: kahkonen m. Cancer Res. 2005 Sep 15;65(18):8101-10. doi: 10.1158/0008-5472.CAN-04-0366. Cancer Res. 2005. PMID: 16166283

10

[X-chromosome-linked mental deficiency and the chromosome marker fra(X)(q28)].

Simola KO, Kähkönen M, Leisti J. Simola KO, et al. Among authors: kahkonen m. Duodecim. 1982;98(7):526-34. Duodecim. 1982. PMID: 6953010 Finnish. No abstract available.

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