Forsius H - 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. Among authors: forsius h. Am J Hum Genet. 1988 Oct;43(4):476-83. Am J Hum Genet. 1988. PMID: 3177388 Free PMC article.

2

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: forsius h. Eur J Hum Genet. 1999 Apr;7(3):368-76. doi: 10.1038/sj.ejhg.5200300. Eur J Hum Genet. 1999. PMID: 10234514

3

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: forsius h. Ann Hum Genet. 1999 Nov;63(Pt 6):521-33. doi: 10.1017/S0003480099007812. Ann Hum Genet. 1999. PMID: 11246454

4

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. Among authors: forsius h. Am J Hum Genet. 1991 Jan;48(1):31-8. Am J Hum Genet. 1991. PMID: 1985461 Free PMC article.

5

Haplotype and multipoint linkage analysis in Finnish choroideremia families.

Sankila EM, Lehner T, Eriksson AW, Forsius H, Kärnä J, Page D, Ott J, de la Chapelle A. Sankila EM, et al. Among authors: forsius h. Hum Genet. 1989 Dec;84(1):66-70. doi: 10.1007/BF00210674. Hum Genet. 1989. PMID: 2575071

6

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. Among authors: forsius h. Clin Genet. 1987 Sep;32(3):192-5. doi: 10.1111/j.1399-0004.1987.tb03353.x. Clin Genet. 1987. PMID: 2887320

7

Sex ratio and proportion of affected sons in sibships with X-chromosomal recessive traits: maximum likelihood estimation in truncated multinomial distributions.

Fellman J, Eriksson AW, Forsius H. Fellman J, et al. Among authors: forsius h. Hum Hered. 2002;53(4):173-80. doi: 10.1159/000066191. Hum Hered. 2002. PMID: 12435881

8

Association of LOXL1 gene with Finnish exfoliation syndrome patients.

Lemmelä S, Forsman E, Onkamo P, Nurmi H, Laivuori H, Kivelä T, Puska P, Heger M, Eriksson A, Forsius H, Järvelä I. Lemmelä S, et al. Among authors: forsius h. J Hum Genet. 2009 May;54(5):289-97. doi: 10.1038/jhg.2009.28. Epub 2009 Apr 3. J Hum Genet. 2009. PMID: 19343041

9

Wolman disease: morphological, clinical and genetic studies on the first Scandinavian cases.

Röyttä M, Fagerlund AS, Toikkanen S, Salmi TT, Jorde LB, Forsius HR, Eriksson AW. Röyttä M, et al. Among authors: forsius hr. Clin Genet. 1992 Jul;42(1):1-7. doi: 10.1111/j.1399-0004.1992.tb03125.x. Clin Genet. 1992. PMID: 1516222

10

Pseudoinflammatory fundus dystrophy: a follow-up study.

Eriksson AW, Suvanto EA, Frants RR, Forsius HR. Eriksson AW, et al. Among authors: forsius hr. Clin Genet. 1990 Jul;38(1):21-32. doi: 10.1111/j.1399-0004.1990.tb03543.x. Clin Genet. 1990. PMID: 2387082

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