Salo PJ - Search Results

1

Recurrent duplication and deletion polymorphisms on the long arm of the Y chromosome in normal males.

Jobling MA, Samara V, Pandya A, Fretwell N, Bernasconi B, Mitchell RJ, Gerelsaikhan T, Dashnyam B, Sajantila A, Salo PJ, Nakahori Y, Disteche CM, Thangaraj K, Singh L, Crawford MH, Tyler-Smith C. Jobling MA, et al. Among authors: salo pj. Hum Mol Genet. 1996 Nov;5(11):1767-75. doi: 10.1093/hmg/5.11.1767. Hum Mol Genet. 1996. PMID: 8923005

2

Genetic relationships of Asians and Northern Europeans, revealed by Y-chromosomal DNA analysis.

Zerjal T, Dashnyam B, Pandya A, Kayser M, Roewer L, Santos FR, Schiefenhövel W, Fretwell N, Jobling MA, Harihara S, Shimizu K, Semjidmaa D, Sajantila A, Salo P, Crawford MH, Ginter EK, Evgrafov OV, Tyler-Smith C. Zerjal T, et al. Am J Hum Genet. 1997 May;60(5):1174-83. Am J Hum Genet. 1997. PMID: 9150165 Free PMC article.

3

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. Hum Genet. 1995 Mar;95(3):283-6. doi: 10.1007/BF00225194. Hum Genet. 1995. PMID: 7868119

4

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. 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.

5

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. Genes Chromosomes Cancer. 1995 Nov;14(3):210-4. doi: 10.1002/gcc.2870140309. Genes Chromosomes Cancer. 1995. PMID: 8589038

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

Diverse spermatogenic defects in humans caused by Y chromosome deletions encompassing a novel RNA-binding protein gene.

Reijo R, Lee TY, Salo P, Alagappan R, Brown LG, Rosenberg M, Rozen S, Jaffe T, Straus D, Hovatta O, et al. Reijo R, et al. Nat Genet. 1995 Aug;10(4):383-93. doi: 10.1038/ng0895-383. Nat Genet. 1995. PMID: 7670487

8

Comparison of PCR assay with bacterial culture for detecting Streptococcus pneumoniae in middle ear fluid of children with acute otitis media.

Virolainen A, Salo P, Jero J, Karma P, Eskola J, Leinonen M. Virolainen A, et al. J Clin Microbiol. 1994 Nov;32(11):2667-70. doi: 10.1128/jcm.32.11.2667-2670.1994. J Clin Microbiol. 1994. PMID: 7852553 Free PMC article.

9

Diagnosis of bacteremic pneumococcal pneumonia by amplification of pneumolysin gene fragment in serum.

Salo P, Ortqvist A, Leinonen M. Salo P, et al. J Infect Dis. 1995 Feb;171(2):479-82. doi: 10.1093/infdis/171.2.479. J Infect Dis. 1995. PMID: 7844395

10

PCR assay for detecting Streptococcus pneumoniae in the middle ear of children with otitis media with effusion.

Jero J, Virolainen A, Salo P, Leinonen M, Eskola J, Karma P. Jero J, et al. Acta Otolaryngol. 1996 Mar;116(2):288-92. doi: 10.3109/00016489609137843. Acta Otolaryngol. 1996. PMID: 8725534

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