Výsledky vyhledávání - Lourenco, Teresa

Neonatal Marfan syndrome: a successful early multidisciplinary approach Autor Amado, Marta, Calado, Maria Angelina, Ferreira, Rui, Lourenço, Teresa

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Molecular characterization of a rare analphoid supernumerary marker chromosome derived from 7q35 → qter: a case report Autor Marques, Bárbara, Ferreira, Cristina, Brito, Filomena, Pedro, Sónia, Alves, Cristina, Lourenço, Teresa, Amorim, Marta, Correia, Hildeberto

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Deletions within COL11A1 in Type 2 stickler syndrome detected by multiplex ligation-dependent probe amplification (MLPA) Autor Vijzelaar, Raymon, Waller, Sarah, Errami, Abdellatif, Donaldson, Alan, Lourenco, Teresa, Rodrigues, Marcia, McConnell, Vivienne, Fincham, Gregory, Snead, Martin, Richards, Allan

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Urinary Tract Effects of HPSE2 Mutations Autor Stuart, Helen M., Roberts, Neil A., Hilton, Emma N., McKenzie, Edward A., Daly, Sarah B., Hadfield, Kristen D., Rahal, Jeffery S., Gardiner, Natalie J., Tanley, Simon W., Lewis, Malcolm A., Sites, Emily, Angle, Brad, Alves, Cláudia, Lourenço, Teresa, Rodrigues, Márcia, Calado, Angelina, Amado, Marta, Guerreiro, Nancy, Serras, Inês, Beetz, Christian, Varga, Rita-Eva, Silay, Mesrur Selcuk, Darlow, John M., Dobson, Mark G., Barton, David E., Hunziker, Manuela, Puri, Prem, Feather, Sally A., Goodship, Judith A., Goodship, Timothy H.J., Lambert, Heather J., Cordell, Heather J., Saggar, Anand, Kinali, Maria, Lorenz, Christian, Moeller, Kristina, Schaefer, Franz, Bayazit, Aysun K., Weber, Stefanie, Newman, William G., Woolf, Adrian S.

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