Alitalo T - Search Results

1

Linkage relationships and gene order around the locus for X-linked retinoschisis.

Alitalo T, Forsius H, Kärnä J, Frants RR, Eriksson AW, Wood S, Kruse TA, de la Chapelle A. Alitalo T, et al. Am J Hum Genet. 1988 Oct;43(4):476-83. Am J Hum Genet. 1988. PMID: 3177388 Free PMC article.

2

X-linked retinoschisis is closely linked to DXS41 and DXS16 but not DXS85.

Alitalo T, Kärnä J, Forsius H, de la Chapelle A. Alitalo T, et al. Clin Genet. 1987 Sep;32(3):192-5. doi: 10.1111/j.1399-0004.1987.tb03353.x. Clin Genet. 1987. PMID: 2887320

3

Molecular characterization of a Y;15 translocation segregating in a family.

Alitalo T, Tiihonen J, Hakola P, de la Chapelle A. Alitalo T, et al. Hum Genet. 1988 May;79(1):29-35. doi: 10.1007/BF00291705. Hum Genet. 1988. PMID: 3366460

4

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: alitalo t. Am J Hum Genet. 1997 May;60(5):1139-49. Am J Hum Genet. 1997. PMID: 9150161 Free PMC article.

5

Three widespread founder mutations contribute to high incidence of X-linked juvenile retinoschisis in Finland.

Huopaniemi L, Rantala A, Forsius H, Somer M, de la Chapelle A, Alitalo T. Huopaniemi L, et al. Among authors: alitalo t. Eur J Hum Genet. 1999 Apr;7(3):368-76. doi: 10.1038/sj.ejhg.5200300. Eur J Hum Genet. 1999. PMID: 10234514

6

Skewed secondary sex ratio in the offspring of carriers of the 214G > A mutation of the RS1 gene.

Huopaniemi L, Fellman J, Rantala A, Eriksson A, Forsius H, De La Chapelle A, Alitalo T. Huopaniemi L, et al. Among authors: alitalo t. Ann Hum Genet. 1999 Nov;63(Pt 6):521-33. doi: 10.1017/S0003480099007812. Ann Hum Genet. 1999. PMID: 11246454

7

Genetic mapping of 12 marker loci in the Xp22.3-p21.2 region.

Alitalo T, Kruse TA, Ahrens P, Albertsen HM, Eriksson AW, de la Chapelle A. Alitalo T, et al. Hum Genet. 1991 Apr;86(6):599-603. doi: 10.1007/BF00201548. Hum Genet. 1991. PMID: 1673960

8

Localization of the Aland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysis.

Alitalo T, Kruse TA, Forsius H, Eriksson AW, de la Chapelle A. Alitalo T, et al. Am J Hum Genet. 1991 Jan;48(1):31-8. Am J Hum Genet. 1991. PMID: 1985461 Free PMC article.

9

Refined localization of the gene causing X-linked juvenile retinoschisis.

Alitalo T, Kruse TA, de la Chapelle A. Alitalo T, et al. Genomics. 1991 Mar;9(3):505-10. doi: 10.1016/0888-7543(91)90417-d. Genomics. 1991. PMID: 2032721

10

Determination of the breakpoints of 1;7 translocations in myelodysplastic syndrome by in situ hybridization using chromosome-specific alpha satellite DNA from human chromosomes 1 and 7.

Alitalo T, Willard HF, de la Chapelle A. Alitalo T, et al. Cytogenet Cell Genet. 1989;50(1):49-53. doi: 10.1159/000132718. Cytogenet Cell Genet. 1989. PMID: 2743817

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