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Page 1
The r(20) syndrome.
Herva R, Saarinen I, Leikkonen L. Herva R, et al. Among authors: saarinen i. J Med Genet. 1977 Aug;14(4):281-3. doi: 10.1136/jmg.14.4.281. J Med Genet. 1977. PMID: 926142 Free PMC article.
Dicentric Y chromosome arising via tandem translocation.
Herva R, Saarinen I, Savikurki H, de la Chapelle A. Herva R, et al. Among authors: saarinen i. Am J Med Genet. 1980;7(2):115-22. doi: 10.1002/ajmg.1320070205. Am J Med Genet. 1980. PMID: 7193412
Two true hermaphrodites with XX chromosomes.
Gripenberg U, Saarinen I, Bwibo NO, Oduori ML, Grayburn JA, Awori NW, Wasunna AE, Kinuthia DM. Gripenberg U, et al. Among authors: saarinen i. East Afr Med J. 1978 Aug;55(8):373-9. East Afr Med J. 1978. PMID: 699853 No abstract available.
Bone-marrow chromosomes in healthy subjects.
Knuutila S, Simell O, Lipponen P, Saarinen I. Knuutila S, et al. Among authors: saarinen i. Hereditas. 1976;82(1):29-35. doi: 10.1111/j.1601-5223.1976.tb01534.x. Hereditas. 1976. PMID: 1262236 Free article. No abstract available.
Diagnostic yield of genetic testing in a multinational heterogeneous cohort of 2088 DCM patients.
Heliö K, Cicerchia M, Hathaway J, Tommiska J, Huusko J, Saarinen I, Koskinen L, Muona M, Kytölä V, Djupsjöbacka J, Gentile M, Salmenperä P, Alastalo TP, Steinberg C, Heliö T, Paananen J, Myllykangas S, Koskenvuo J. Heliö K, et al. Among authors: saarinen i. Front Cardiovasc Med. 2023 Sep 19;10:1254272. doi: 10.3389/fcvm.2023.1254272. eCollection 2023. Front Cardiovasc Med. 2023. PMID: 37795486 Free PMC article.
Correction to: Diagnostic utility of next-generation sequencing-based panel testing in 543 patients with suspected skeletal dysplasia.
Scocchia A, Kangas-Kontio T, Irving M, Hero M, Saarinen I, Pelttari L, Gall K, Valo S, Huusko JM, Tallila J, Sistonen J, Koskenvuo J, Alastalo TP. Scocchia A, et al. Among authors: saarinen i. Orphanet J Rare Dis. 2022 Feb 17;17(1):59. doi: 10.1186/s13023-022-02242-8. Orphanet J Rare Dis. 2022. PMID: 35177119 Free PMC article. No abstract available.
Prevalence of RPGR-Mediated Retinal Dystrophy in an Unselected Cohort of Over 5000 Patients.
Tuupanen S, Gall K, Sistonen J, Saarinen I, Kämpjärvi K, Wells K, Merkkiniemi K, von Nandelstadh P, Sarantaus L, Känsäkoski J, Mårtenson E, Västinsalo H, Schleit J, Sankila EM, Kere A, Junnila H, Siivonen P, Andreevskaya M, Kytölä V, Muona M, Salmenperä P, Myllykangas S, Koskenvuo J, Alastalo TP. Tuupanen S, et al. Among authors: saarinen i. Transl Vis Sci Technol. 2022 Jan 3;11(1):6. doi: 10.1167/tvst.11.1.6. Transl Vis Sci Technol. 2022. PMID: 34985506 Free PMC article.
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