"Pure" partial trisomy 4q25-qter owing to a de novo 4;22 translocation von Mikelsaar, R V, Lurie, I W, Ilus, T E

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Mosaic terminal del(19)(q13.33:) in a girl with seizures and mental retardation von MIKELSAAR, RUTH V, VARB, KADI, SÜVARI, ANNELI, SCHINZEL, ALBERT

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Atypical case of Aarskog syndrome von Mikelsaar, R V, Lurie, I W

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Neonatal Thyroid-Stimulating Hormone Screening as an Indirect Method for the Assessment of Iodine Deficiency in Estonia von Mikelsaar, Ruth V., Viikmaa, Mart

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Neonatal screening for congenital hypothyroidism in Estonia von Mikelsaar, R V, Zordania, R, Viikmaa, M, Kudrjavtseva, G

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Distal trisomy 14q von Mikelsaar, R V, Ilus, T A, Lurie, I W

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Dermal Patterns in Normal Estonians von Horn, A. V., Mikelsaar, R. V.-A.

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A case of trisomy for the short arm of chromosome no. 9(+9(p)) von Käosaar, M E, Mikelsaar, A V, Talvik, T A, Mikelsaar, R V

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Mosaic terminal del(19)(q13.33:) in a girl with seizures and mental retardation von Mikelsaar, R V, Varb, K, Süvari, A, Schinzel, A

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Neutralization of Clostridium difficile Toxin B Mediated by Engineered Lactobacilli That Produce Single-Domain Antibodies von Andersen, Kasper Krogh, Strokappe, Nika M, Hultberg, Anna, Truusalu, Kai, Smidt, Imbi, Mikelsaar, Raik-Hiio, Mikelsaar, Marika, Verrips, Theo, Hammarström, Lennart, Marcotte, Harold

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Psoriasis vulgaris in a male with partial deletion 18p von Mikelsaar, Ruth V., Muru, Kai, Kulla, Andres, Süvari, Anneli

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Neonatal Screening in Europe Revisited: An ISNS Perspective on the Current State and Developments Since 2010 von Loeber, J Gerard, Platis, Dimitris, Zetterström, Rolf H, Almashanu, Shlomo, Boemer, François, Bonham, James R, Borde, Patricia, Brincat, Ian, Cheillan, David, Dekkers, Eugenie, Dimitrov, Dobry, Fingerhut, Ralph, Franzson, Leifur, Groselj, Urh, Hougaard, David, Knapkova, Maria, Kocova, Mirjana, Kotori, Vjosa, Kozich, Viktor, Kremezna, Anastasiia, Kurkijärvi, Riikka, La Marca, Giancarlo, Mikelsaar, Ruth, Milenkovic, Tatjana, Mitkin, Vyacheslav, Moldovanu, Florentina, Ceglarek, Uta, O'Grady, Loretta, Oltarzewski, Mariusz, Pettersen, Rolf D, Ramadza, Danijela, Salimbayeva, Damilya, Samardzic, Mira, Shamsiddinova, Markhabo, Songailiené, Jurgita, Szatmari, Ildiko, Tabatadze, Nazi, Tezel, Basak, Toromanovic, Alma, Tovmasyan, Irina, Usurelu, Natalia, Vevere, Parsla, Vilarinho, Laura, Vogazianos, Marios, Yahyaoui, Raquel, Zeyda, Maximilian, Schielen, Peter C J I

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Polymorphic Glutathione S-transferase M1 is a Risk Factor of Primary Open-angle Glaucoma among Estonians von Juronen, Erkki, Tasa, Gunnar, Veromann, Siiri, Parts, Lii, Tiidla, Anne, Pulges, Riina, Panov, Aleksei, Soovere, Leili, Koka, Külle, Mikelsaar, Aavo-Valdur

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Polymorphic Glutathione S-Transferases as Genetic Risk Factors for Senile Cortical Cataract in Estonians von Juronen, Erkki, Tasa, Gunnar, Veromann, Siiri, Parts, Lii, Tiidla, Anne, Pulges, Riina, Panov, Aleksei, Soovere, Leili, Koka, Kulle, Mikelsaar, Aavo-Valdur

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Titin A-band-specific monoclonal antibody Tit1 5H1.1. Cellular Titin as a centriolar protein in non-muscle cells von Mikelsaar, Aavo-Valdur, Sünter, Alar, Toomik, Peeter, Mikelsaar, Ruth, Kalev, Ingrid, Kõiveer, Anu, Piirsoo, Andres, Karpson, Kalmer, Juronen, Erkki

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Y-chromosomal diversity in Europe is clinal and influenced primarily by geography, rather than by language von Rosser, Z.H, Zerjal, T, Hurles, M.E, Adojaan, M, Alavantic, D, Amorim, A, Amos, W, Armenteros, M, Arroyo, E, Barbujani, G, Beckman, G, Beckman, L, Bertranpetit, J, Bosch, E, Bradley, D.G, Brede, G, Cooper, Graeme, Côrte-Real, H.B, de Knijff, P, Decorte, Ronny, Dubrova, Y.E, Evgrafov, O, Gilissen, A, Glisic, S, Gölge, M, Hill, E.W, Jeziorowska, A, Kalaydjieva, L, Kayser, M, Kivisild, T, Kravchenko, S.A, Krumina, A, Kucinskas, V, Lavinha, J, Livshits, L.A, Malaspina, P, Maria, S, McElreavey, K, Meitinger, T.A, Mikelsaar, A.V, Mitchell, R.J, Nafa, K, Nicholson, J, Nørby, S, Pandya, A, Parik, J, Patsalis, P.C, Pereira, L, Peterlin, B, Pielberg, G, Prata, M.J, Previderé, C, Roewer, L, Rootsi, S, Rubinsztein, D.C, Saillard, J, Santos, F.R, Stefanescu, G, Sykes, B.C, Tolun, A, Villems, R, Tyler-Smith, C, Jobling, M.A

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A 4p- syndrome: A case report von Mikelsaar, A.-V. N., Lazjuk, G. J., Lurie, J. W., T r, S., K osaar, M. E., Mikelsaar, Raik, Loolaid, V. E.

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Amniotic Fluid Microflora in Asymptomatic Women At Mid-Gestation von MÄNDAR, Reet, LOIVUKENE, Krista, EHRENBERG, Aivar, SMIDT, Imbi, RAUKAS, Elve, KASK, Virve, MIKELSAAR, Marika

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Inherited translocations in two families (t(14q+;10q?) and t(13q?;21q+)) von Talvik, T., Mikelsaar, A.-V., Mikelsaar, Ruth, K osaar, M., T r, S.

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1q+ variants in a normal adult population (one with a pericentric inversion) von T r, S., K osaar, M., Mikelsaar, A.-V.

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