Paavola P - Search Results

1

Genetic analysis in Finnish families with inflammatory bowel disease supports linkage to chromosome 3p21.

Paavola P, Heliö T, Kiuru M, Halme L, Turunen U, Terwilliger J, Karvonen AL, Julkunen R, Niemelä S, Nurmi H, Färkkilä M, Kontula K. Paavola P, et al. Eur J Hum Genet. 2001 May;9(5):328-34. doi: 10.1038/sj.ejhg.5200626. Eur J Hum Genet. 2001. PMID: 11378820

2

Familial and sporadic inflammatory bowel disease: comparison of clinical features and serological markers in a genetically homogeneous population.

Halme L, Turunen U, Heliö T, Paavola P, Walle T, Miettinen A, Järvinen H, Kontula K, Färkkilä M. Halme L, et al. Among authors: paavola p. Scand J Gastroenterol. 2002 Jun;37(6):692-8. doi: 10.1080/00365520212511. Scand J Gastroenterol. 2002. PMID: 12126248

3

[What is known about genetic factors behind chronic inflammatory bowel diseases?].

Heliö T, Paavola P, Halme L, Turunen U, Färkkilä M, Kontula K. Heliö T, et al. Among authors: paavola p. Duodecim. 2000;116(7):713-8. Duodecim. 2000. PMID: 12078137 Review. Finnish. No abstract available.

4

Clinical and genetic heterogeneity in Meckel syndrome.

Paavola P, Salonen R, Baumer A, Schinzel A, Boyd PA, Gould S, Meusburger H, Tenconi R, Barnicoat A, Winter R, Peltonen L. Paavola P, et al. Hum Genet. 1997 Nov;101(1):88-92. doi: 10.1007/s004390050592. Hum Genet. 1997. PMID: 9385376

5

The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24.

Paavola P, Salonen R, Weissenbach J, Peltonen L. Paavola P, et al. Nat Genet. 1995 Oct;11(2):213-5. doi: 10.1038/ng1095-213. Nat Genet. 1995. PMID: 7550354

6

Assignment of the locus for hydrolethalus syndrome to a highly restricted region on 11q23-25.

Visapää I, Salonen R, Varilo T, Paavola P, Peltonen L. Visapää I, et al. Among authors: paavola p. Am J Hum Genet. 1999 Oct;65(4):1086-95. doi: 10.1086/302603. Am J Hum Genet. 1999. PMID: 10486328 Free PMC article.

7

Meckel syndrome.

Salonen R, Paavola P. Salonen R, et al. Among authors: paavola p. J Med Genet. 1998 Jun;35(6):497-501. doi: 10.1136/jmg.35.6.497. J Med Genet. 1998. PMID: 9643292 Free PMC article. Review.

8

High-resolution physical and genetic mapping of the critical region for Meckel syndrome and Mulibrey Nanism on chromosome 17q22-q23.

Paavola P, Avela K, Horelli-Kuitunen N, Bärlund M, Kallioniemi A, Idänheimo N, Kyttälä M, de la Chapelle A, Palotie A, Lehesjoki AE, Peltonen L. Paavola P, et al. Genome Res. 1999 Mar;9(3):267-76. Genome Res. 1999. PMID: 10077533 Free PMC article.

9

Characterization of the lysinuric protein intolerance (LPI) region within T-cell receptor alpha/delta gene cluster on chromosome site 14q11.

Lauteala T, Mykkänen J, Horelli-Kuitunen N, Aaltonen J, Paavola P, Savontaus ML, Simell O, Aula P. Lauteala T, et al. Among authors: paavola p. Hereditas. 1999;130(1):19-24. doi: 10.1111/j.1601-5223.1999.00019.x. Hereditas. 1999. PMID: 10364825 Free article.

10

Molecular cytogenetic mapping of 24 CEPH YACs and 24 gene-specific large insert probes to chromosome 17.

Bärlund M, Nupponen NN, Karhu R, Tanner MM, Paavola P, Kallioniemi OP, Kallioniemi A. Bärlund M, et al. Among authors: paavola p. Cytogenet Cell Genet. 1998;82(3-4):189-91. doi: 10.1159/000015096. Cytogenet Cell Genet. 1998. PMID: 9858813

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