Competitive intramolecular C-C vs. C-O bond coupling reactions toward C6 ring-fused 2-pyridone synthesis von Lepitre, T, Pintiala, C, Muru, K, Comesse, S, Rebbaa, A, Lawson, A M, Daïch, A

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A Boy with Holt-Oram Syndrome Caused by Novel Mutation c.1304delT in the TBX5 Gene von Muru, K., Kalev, I., Teek, R., Sõnajalg, M., Kuuse, K., Reimand, T., Õunap, K.

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A Novel Mutation in the M1S1 Gene Responsible for Gelatinous Droplike Corneal Dystrophy von Tasa, Gunnar, Kals, Jaak, Muru, Kai, Juronen, Erkki, Piirsoo, Andres, Veromann, Siiri, Janes, Silvi, Mikelsaar, Aavo-Valdur, Lang, Aavo

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Competitive intramolecular C-C vs. C-O bond coupling reactions toward C6 ring-fused 2-pyridone synthesisElectronic supplementary information (ESI) available: Experimental data and... von Lepitre, T, Pintiala, C, Muru, K, Comesse, S, Rebbaa, A, Lawson, A. M, Daïch, A

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Competitive intramolecular C–C vs. C–O bond coupling reactions toward C 6 ring-fused 2-pyridone synthesis von Lepitre, T., Pintiala, C., Muru, K., Comesse, S., Rebbaa, A., Lawson, A. M., Daïch, A.

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ChemInform Abstract: Competitive Intramolecular C—C vs. C—O Bond Coupling Reactions Toward C6 Ring‐Fused 2‐Pyridone Synthesis von Lepitre, T., Pintiala, C., Muru, K., Comesse, S., Rebbaa, A., Lawson, A. M., Daich, A.

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A methodology of the satellite mapping and monitoring of protected landscapes in Estonia von Aaviksoo, K, Muru, K

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Bi-allelic loss-of-function variants in WBP4, encoding a spliceosome protein, result in a variable neurodevelopmental syndrome von Engal, E, Oja, KT, Maroofian, R, Geminder, O, Le, TL, Marzin, P, Guimier, A, Mor, E, Zvi, N, Elefant, N, Zaki, MS, Gleeson, JG, Muru, K, Pajusalu, S, Wojcik, MH, Pachat, D, Elmaksoud, MA, Chan Jeong, W, Lee, H, Bauer, P, Zifarelli, G, Houlden, H, Daana, M, Elpeleg, O, Amiel, J, Lyonnet, S, Gordon, CT, Harel, T, Õunap, K, Salton, M, Mor-Shaked, H

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ChemInform Abstract: Competitive Intramolecular C—C vs. C—O Bond Coupling Reactions Toward C 6 Ring‐Fused 2‐Pyridone Synthesis von Lepitre, T., Pintiala, C., Muru, K., Comesse, S., Rebbaa, A., Lawson, A. M., Daich, A.

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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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Vascular disease and apathy symptoms in the very old: A cross‐sectional and longitudinal meta‐analysis of individual participant data von Klei, Veerle M. G. T. H., Poortvliet, Rosalinde K. E., Bogaerts, Jonathan M. K., Blom, Jeanet W., Mooijaart, Simon P., Teh, Ruth, Muru‐Lanning, Marama, Palapar, Leah, Kingston, Andrew, Robinson, Louise, Kerse, Ngaire, Gussekloo, Jacobijn

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Full-field, conformal epiretinal electrode array using hydrogel and polymer hybrid technology von Zhou, Muru, Young, Benjamin K., Valle, Elena della, Koo, Beomseo, Kim, Jinsang, Weiland, James D.

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Rhythmic Patterns of Coastal Formations as Signs of Past Climate Fluctuations on Uplifting Coasts of Estonia, the Baltic Sea von Tõnisson, H, Suursaar, Ü, Kont, A, Muru, M, Rivis, R, Rosentau, A, Tamura, T, Vilumaa, K

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Experimental determination of the lateral dose response functions of detectors to be applied in the measurement of narrow photon-beam dose profiles von Poppinga, D, Meyners, J, Delfs, B, Muru, A, Harder, D, Poppe, B, Looe, HK

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Natural history of KBG syndrome in a large European cohort von Loberti, Lorenzo, Bruno, Lucia Pia, Granata, Stefania, Doddato, Gabriella, Resciniti, Sara, Fava, Francesca, Carullo, Michele, Rahikkala, Elisa, Jouret, Guillaume, Menke, Leonie A, Lederer, Damien, Vrielynck, Pascal, Ryba, Lukáš, Brunetti-Pierri, Nicola, Lasa-Aranzasti, Amaia, Cueto-González, Anna Maria, Trujillano, Laura, Valenzuela, Irene, Tizzano, Eduardo F, Spinelli, Alessandro Mauro, Bruno, Irene, Currò, Aurora, Stanzial, Franco, Benedicenti, Francesco, Lopergolo, Diego, Santorelli, Filippo Maria, Aristidou, Constantia, Tanteles, George A, Maystadt, Isabelle, Tkemaladze, Tinatin, Reimand, Tiia, Lokke, Helen, Õunap, Katrin, Haanpää, Maria K, Holubová, Andrea, Zoubková, Veronika, Schwarz, Martin, Žordania, Riina, Muru, Kai, Roht, Laura, Tihveräinen, Annika, Teek, Rita, Thomson, Ulvi, Atallah, Isis, Superti-Furga, Andrea, Buoni, Sabrina, Canitano, Roberto, Scandurra, Valeria, Rossetti, Annalisa, Grosso, Salvatore, Battini, Roberta, Baldassarri, Margherita, Mencarelli, Maria Antonietta, Rizzo, Caterina Lo, Bruttini, Mirella, Mari, Francesca, Ariani, Francesca, Renieri, Alessandra, Pinto, Anna Maria

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AXIN2‐related oligodontia‐colorectal cancer syndrome with cleft palate as a possible new feature von Roht, Laura, Hyldebrandt, Hanne K., Stormorken, Astrid T., Nordgarden, Hilde, Sijmons, Rolf H., Bos, Dennis K., Riegert‐Johnson, Douglas, Mantia‐Macklin, Sarah, Ilves, Pilvi, Muru, Kai, Wojcik, Monica H., Kahre, Tiina, Õunap, Katrin

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TOPz: Photometric redshifts for J-PAS von Laur, J., Tempel, E., Tamm, A., Kipper, R., Liivamägi, L. J., Hernán-Caballero, A., Muru, M. M., Chaves-Montero, J., Díaz-García, L. A., Turner, S., Tuvikene, T., Queiroz, C., Bom, C. R., Fernández-Ontiveros, J. A., González Delgado, R. M., Civera, T., Abramo, R., Alcaniz, J., Benítez, N., Bonoli, S., Carneiro, S., Cenarro, J., Cristóbal-Hornillos, D., Dupke, R., Ederoclite, A., López-Sanjuan, C., Marín-Franch, A., de Oliveira, C. M., Moles, M., Sodré, L., Taylor, K., Varela, J., Ramió, H. V.

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An ancestral 10-bp repeat expansion in VWA1 causes recessive hereditary motor neuropathy von Pagnamenta, Alistair T, Kaiyrzhanov, Rauan, Zou, Yaqun, Da'as, Sahar I, Maroofian, Reza, Donkervoort, Sandra, Dominik, Natalia, Lauffer, Marlen, Ferla, Matteo P, Orioli, Andrea, Giess, Adam, Tucci, Arianna, Beetz, Christian, Sedghi, Maryam, Ansari, Behnaz, Barresi, Rita, Basiri, Keivan, Cortese, Andrea, Elgar, Greg, Fernandez-Garcia, Miguel A, Yip, Janice, Foley, A Reghan, Gutowski, Nicholas, Jungbluth, Heinz, Lassche, Saskia, Lavin, Tim, Marcelis, Carlo, Marks, Peter, Marini-Bettolo, Chiara, Medne, Livija, Moslemi, Ali-Reza, Sarkozy, Anna, Reilly, Mary M, Muntoni, Francesco, Millan, Francisca, Muraresku, Colleen C, Need, Anna C, Nemeth, Andrea H, Neuhaus, Sarah B, Norwood, Fiona, O'Donnell, Marie, O'Driscoll, Mary, Rankin, Julia, Yum, Sabrina W, Zolkipli-Cunningham, Zarazuela, Brusius, Isabell, Wunderlich, Gilbert, Karakaya, Mert, Wirth, Brunhilde, Fakhro, Khalid A, Tajsharghi, Homa, Bönnemann, Carsten G, Taylor, Jenny C, Houlden, Henry

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FLAD1‐associated multiple acyl‐CoA dehydrogenase deficiency identified by newborn screening von Muru, Kai, Reinson, Karit, Künnapas, Kadi, Lilleväli, Hardo, Nochi, Zahra, Mosegaard, Signe, Pajusalu, Sander, Olsen, Rikke K. J., Õunap, Katrin

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Estonian literature II booklet for class X. 1967 von Lawn, K (author), Light Publishing House (publisher), Buffer, K. (author), Muru, K (autor), Kirjastus Valgus (kirjastaja), Puhvel, K. (autor)

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