Αποτελέσματα αναζήτησης - Rots, Dmitrijs
- Εμφανίζονται 1 - 10 Αποτελέσματα από 10
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Analysis of possible genetic risk factors contributing to development of childhood acute lymphoblastic leukaemia in the Latvian population από Kreile, Madara, Piekuse, Linda, Rots, Dmitrijs, Dobele, Zane, Kovalova, Zhanna, Lace, Baiba
Έκδοση 2016Κείμενο -
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Genetic landscape of preterm birth due to cervical insufficiency: Comprehensive gene analysis and patient next-generation sequencing data interpretation από Volozonoka, Ludmila, Rots, Dmitrijs, Kempa, Inga, Kornete, Anna, Rezeberga, Dace, Gailite, Linda, Miskova, Anna
Έκδοση 2020Κείμενο -
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A Higher Polygenic Risk Score Is Associated with a Higher Recurrence Rate of Atrial Fibrillation in Direct Current Cardioversion-Treated Patients από Vogel, Simon, Rudaka, Irina, Rots, Dmitrijs, Isakova, Jekaterīna, Kalējs, Oskars, Vīksne, Kristīne, Gailīte, Linda
Έκδοση 2021Κείμενο -
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Association of ARID5B Genetic Variants with Risk of Childhood B Cell Precursor Acute Lymphoblastic Leukaemia in Latvia από Kreile, Madara, Rots, Dmitrijs, Zarina, Agnese, Rautiainen, Linda, Visnevska-Preciniece, Zelma, Kovalova, Zhanna, Gailite, Linda
Έκδοση 2018Κείμενο -
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UGT1A1 Variants c.864+5G>T and c.996+2_996+5del of a Crigler-Najjar Patient Induce Aberrant Splicing in Minigene Assays από Gailite, Linda, Valenzuela-Palomo, Alberto, Sanoguera-Miralles, Lara, Rots, Dmitrijs, Kreile, Madara, Velasco, Eladio A.
Έκδοση 2020Κείμενο -
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Novel Variant of the Androgen Receptor Gene in a Patient With Complete Androgen Insensitivity Syndrome and Polyorchidism από Konrade, Ilze, Zavorikina, Julija, Fridvalde, Aija, Rots, Dmitrijs, Kalere, Ieva, Strumfa, Ilze, Dambrova, Maija, Gailite, Linda
Έκδοση 2019Κείμενο -
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Clinical Phenotyping and Biomarkers in Spinal and Bulbar Muscular Atrophy από Millere, Elina, Rots, Dmitrijs, Glazere, Ieva, Taurina, Gita, Kurjane, Natalja, Priedite, Viktorija, Gailite, Linda, Blennow, Kaj, Zetterberg, Henrik, Kenina, Viktorija
Έκδοση 2021Κείμενο -
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Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature από Rots, Dmitrijs, Chater-Diehl, Eric, Dingemans, Alexander J.M., Goodman, Sarah J., Siu, Michelle T., Cytrynbaum, Cheryl, Choufani, Sanaa, Hoang, Ny, Walker, Susan, Awamleh, Zain, Charkow, Joshua, Meyn, Stephen, Pfundt, Rolph, Rinne, Tuula, Gardeitchik, Thatjana, de Vries, Bert B.A., Deden, A. Chantal, Leenders, Erika, Kwint, Michael, Stumpel, Constance T.R.M., Stevens, Servi J.C., Vermeulen, Jeroen R., van Harssel, Jeske V.T., Bosch, Danielle G.M., van Gassen, Koen L.I., van Binsbergen, Ellen, de Geus, Christa M., Brackel, Hein, Hempel, Maja, Lessel, Davor, Denecke, Jonas, Slavotinek, Anne, Strober, Jonathan, Crunk, Amy, Folk, Leandra, Wentzensen, Ingrid M., Yang, Hui, Zou, Fanggeng, Millan, Francisca, Person, Richard, Xie, Yili, Liu, Shuxi, Ousager, Lilian B., Larsen, Martin, Schultz-Rogers, Laura, Morava, Eva, Klee, Eric W., Berry, Ian R., Campbell, Jennifer, Lindstrom, Kristin, Pruniski, Brianna, Neumeyer, Ann M., Radley, Jessica A., Phornphutkul, Chanika, Schmidt, Berkley, Wilson, William G., Õunap, Katrin, Reinson, Karit, Pajusalu, Sander, van Haeringen, Arie, Ruivenkamp, Claudia, Cuperus, Roos, Santos-Simarro, Fernando, Palomares-Bralo, María, Pacio-Míguez, Marta, Ritter, Alyssa, Bhoj, Elizabeth, Tønne, Elin, Tveten, Kristian, Cappuccio, Gerarda, Brunetti-Pierri, Nicola, Rowe, Leah, Bunn, Jason, Saenz, Margarita, Platzer, Konrad, Mertens, Mareike, Caluseriu, Oana, Nowaczyk, Małgorzata J.M., Cohn, Ronald D., Kannu, Peter, Alkhunaizi, Ebba, Chitayat, David, Scherer, Stephen W., Brunner, Han G., Vissers, Lisenka E.L.M., Kleefstra, Tjitske, Koolen, David A., Weksberg, Rosanna
Έκδοση 2021Κείμενο