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Prevalence of c.35delG and p.M34T mutations in the GJB2 gene in Estonia.
Teek R, Kruustük K, Zordania R, Joost K, Reimand T, Möls T, Oitmaa E, Kahre T, Tõnisson N, Ounap K. Teek R, et al. Among authors: tonisson n. Int J Pediatr Otorhinolaryngol. 2010 Sep;74(9):1007-12. doi: 10.1016/j.ijporl.2010.05.026. Epub 2010 Jun 18. Int J Pediatr Otorhinolaryngol. 2010. PMID: 20708129
Molecular diagnosis of Down syndrome using quantitative APEX-2 microarrays.
Oitmaa E, Peters M, Vaidla K, Andreson R, Mägi R, Slavin G, Velthut A, Tõnisson N, Reimand T, Remm M, Schneider M, Ounap K, Salumets A, Metspalu A. Oitmaa E, et al. Among authors: tonisson n. Prenat Diagn. 2010 Dec;30(12-13):1170-7. doi: 10.1002/pd.2639. Prenat Diagn. 2010. PMID: 20949644
Prenatal diagnosis of a 46,XY karyotype female fetus with an SRY-associated gonadal dysgenesis, conceived through an intracytoplasmic sperm injection: a case report.
Zhytnik L, Peters M, Tilk K, Reimand T, Ilisson P, Kahre T, Murumets Ü, Ehrenberg A, Ustav EL, Tõnisson N, Mölder S, Teder H, Krjutškov K, Salumets A. Zhytnik L, et al. Among authors: tonisson n. BMC Pregnancy Childbirth. 2022 Feb 5;22(1):105. doi: 10.1186/s12884-022-04431-6. BMC Pregnancy Childbirth. 2022. PMID: 35123446 Free PMC article.
44 results