Tahvanainen E - Search Results

1

Muscle-eye-brain disease and Fukuyama type congenital muscular dystrophy are not allelic.

Ranta S, Pihko H, Santavuori P, Tahvanainen E, de la Chapelle A. Ranta S, et al. Among authors: tahvanainen e. Neuromuscul Disord. 1995 May;5(3):221-5. doi: 10.1016/0960-8966(94)00058-h. Neuromuscul Disord. 1995. PMID: 7633187

2

Selective intestinal malabsorption of vitamin B12 displays recessive mendelian inheritance: assignment of a locus to chromosome 10 by linkage.

Aminoff M, Tahvanainen E, Gräsbeck R, Weissenbach J, Broch H, de la Chapelle A. Aminoff M, et al. Among authors: tahvanainen e. Am J Hum Genet. 1995 Oct;57(4):824-31. Am J Hum Genet. 1995. PMID: 7573042 Free PMC article.

3

Cornea plana congenita gene assigned to the long arm of chromosome 12 by linkage analysis.

Tahvanainen E, Forsius H, Karila E, Ranta S, Eerola M, Weissenbach J, Sistonen P, de la Chapelle A. Tahvanainen E, et al. Genomics. 1995 Mar 20;26(2):290-3. doi: 10.1016/0888-7543(95)80213-6. Genomics. 1995. PMID: 7601455

4

Cohen syndrome gene assigned to the long arm of chromosome 8 by linkage analysis.

Tahvanainen E, Norio R, Karila E, Ranta S, Weissenbach J, Sistonen P, de la Chapelle A. Tahvanainen E, et al. Nat Genet. 1994 Jun;7(2):201-4. doi: 10.1038/ng0694-201. Nat Genet. 1994. PMID: 7920642

5

The gene for a recessively inherited human childhood progressive epilepsy with mental retardation maps to the distal short arm of chromosome 8.

Tahvanainen E, Ranta S, Hirvasniemi A, Karila E, Leisti J, Sistonen P, Weissenbach J, Lehesjoki AE, de la Chapelle A. Tahvanainen E, et al. Proc Natl Acad Sci U S A. 1994 Jul 19;91(15):7267-70. doi: 10.1073/pnas.91.15.7267. Proc Natl Acad Sci U S A. 1994. PMID: 8041778 Free PMC article.

6

Dominantly and recessively inherited cornea plana congenita map to the same small region of chromosome 12.

Tahvanainen E, Villanueva AS, Forsius H, Salo P, de la Chapelle A. Tahvanainen E, et al. Genome Res. 1996 Apr;6(4):249-54. doi: 10.1101/gr.6.4.249. Genome Res. 1996. PMID: 8723718 Free article.

7

Linkage disequilibrium mapping of the cornea plana congenita gene CNA2.

Tahvanainen E, Forsius H, Damsten M, Karila E, Kolehmainen J, Weissenbach J, Sistonen P, de la Chapelle A. Tahvanainen E, et al. Genomics. 1995 Dec 10;30(3):409-14. doi: 10.1006/geno.1995.1258. Genomics. 1995. PMID: 8825624

8

The genetics of cornea plana congenita.

Tahvanainen E, Forsius H, Kolehmainen J, Damsten M, Fellman J, de la Chapelle A. Tahvanainen E, et al. J Med Genet. 1996 Feb;33(2):116-9. doi: 10.1136/jmg.33.2.116. J Med Genet. 1996. PMID: 8929947 Free PMC article.

9

Linkage disequilibrium and physical mapping of X-linked juvenile retinoschisis.

Huopaniemi L, Rantala A, Tahvanainen E, de la Chapelle A, Alitalo T. Huopaniemi L, et al. Among authors: tahvanainen e. Am J Hum Genet. 1997 May;60(5):1139-49. Am J Hum Genet. 1997. PMID: 9150161 Free PMC article.

10

Refined mapping of the Cohen syndrome gene by linkage disequilibrium.

Kolehmainen J, Norio R, Kivitie-Kallio S, Tahvanainen E, de la Chapelle A, Lehesjoki AE. Kolehmainen J, et al. Among authors: tahvanainen e. Eur J Hum Genet. 1997 Jul-Aug;5(4):206-13. Eur J Hum Genet. 1997. PMID: 9359041

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