Kääriäinen H - Search Results

1

Deletion mapping of stature determinants on the long arm of the Y chromosome.

Salo P, Kääriäinen H, Page DC, de la Chapelle A. Salo P, et al. Among authors: kaariainen h. Hum Genet. 1995 Mar;95(3):283-6. doi: 10.1007/BF00225194. Hum Genet. 1995. PMID: 7868119

2

Assignment of an Usher syndrome type III (USH3) gene to chromosome 3q.

Sankila EM, Pakarinen L, Kääriäinen H, Aittomäki K, Karjalainen S, Sistonen P, de la Chapelle A. Sankila EM, et al. Among authors: kaariainen h. Hum Mol Genet. 1995 Jan;4(1):93-8. doi: 10.1093/hmg/4.1.93. Hum Mol Genet. 1995. PMID: 7711740

3

Clinical features of nine males with molecularly defined deletions of the Y chromosome long arm.

Salo P, Ignatius J, Simola KO, Tahvanainen E, Kääriäinen H. Salo P, et al. Among authors: kaariainen h. J Med Genet. 1995 Sep;32(9):711-5. doi: 10.1136/jmg.32.9.711. J Med Genet. 1995. PMID: 8544191 Free PMC article. Review.

4

Molecular mapping of the putative gonadoblastoma locus on the Y chromosome.

Salo P, Kääriäinen H, Petrovic V, Peltomäki P, Page DC, de la Chapelle A. Salo P, et al. Among authors: kaariainen h. Genes Chromosomes Cancer. 1995 Nov;14(3):210-4. doi: 10.1002/gcc.2870140309. Genes Chromosomes Cancer. 1995. PMID: 8589038

5

Genetic control of serum IgE levels and asthma: linkage and linkage disequilibrium studies in an isolated population.

Laitinen T, Kauppi P, Ignatius J, Ruotsalainen T, Daly MJ, Kääriäinen H, Kruglyak L, Laitinen H, de la Chapelle A, Lander ES, Laitinen LA, Kere J. Laitinen T, et al. Among authors: kaariainen h. Hum Mol Genet. 1997 Nov;6(12):2069-76. doi: 10.1093/hmg/6.12.2069. Hum Mol Genet. 1997. PMID: 9328470

6

Microdeletions in patients with X-linked muscular dystrophy: molecular-clinical correlations.

Lindlöf M, Kääriäinen H, van Ommen GJ, de la Chapelle A. Lindlöf M, et al. Among authors: kaariainen h. Clin Genet. 1988 Feb;33(2):131-9. doi: 10.1111/j.1399-0004.1988.tb03424.x. Clin Genet. 1988. PMID: 3162851

7

Genetic counselling in Duchenne and Becker muscular dystrophy is problematic when carrier studies give controversial results.

Kääriäinen H, Lindlöf M, Somer H, de la Chapelle A. Kääriäinen H, et al. Clin Genet. 1990 Mar;37(3):179-87. doi: 10.1111/j.1399-0004.1990.tb03500.x. Clin Genet. 1990. PMID: 1969777

8

A European research conference on the inherited disorders and their genes in different European populations.

de la Chapelle A, Harper P, Kääriäinen H, Norio R. de la Chapelle A, et al. Among authors: kaariainen h. Eur J Hum Genet. 1994;2(3):191-2. doi: 10.1159/000472363. Eur J Hum Genet. 1994. PMID: 7834279 No abstract available.

9

Familial pericentric inversion inv(8)(p23q11).

Boyd H, Kaste J, Hovi E, Ritanen-Mohammed UM, Kääriäinen H, de la Chapelle A, Lehesjoki AE. Boyd H, et al. Among authors: kaariainen h. J Med Genet. 1994 Mar;31(3):201-5. doi: 10.1136/jmg.31.3.201. J Med Genet. 1994. PMID: 8014967 Free PMC article.

10

Molecular studies in Finnish patients with familial juvenile nephronophthisis exclude a founder effect and support a common mutation causing mechanism.

Ala-Mello S, Sankila EM, Koskimies O, de la Chapelle A, Kääriäinen H. Ala-Mello S, et al. Among authors: kaariainen h. J Med Genet. 1998 Apr;35(4):279-83. doi: 10.1136/jmg.35.4.279. J Med Genet. 1998. PMID: 9598719 Free PMC article.

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