Screening of genetic alterations related to non-syndromic hearing loss using MassARRAY iPLEX® technology von Svidnicki, Maria Carolina Costa Melo, Silva-Costa, Sueli Matilde, Ramos, Priscila Zonzini, dos Santos, Nathalia Zocal Pereira, Martins, Fábio Tadeu Arrojo, Castilho, Arthur Menino, Sartorato, Edi Lúcia

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A rare case of deafness and renal abnormalities in HDR syndrome caused by a de novo mutation in the GATA3 gene von Martins, Fábio Tadeu Arrojo, Ramos, Berenice Dias, Sartorato, Edi Lúcia

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Optimization of simultaneous screening of the main mutations involved in non-syndromic deafness using the TaqMan® OpenArray™ Genotyping platform von Martins, Fábio Tadeu Arrojo, Ramos, Priscila Zonzini, Svidnicki, Maria Carolina Costa Melo, Castilho, Arthur Menino, Sartorato, Edi Lúcia

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Searching for digenic inheritance in deaf Brazilian individuals using the multiplex ligation-dependent probe amplification technique von da Silva-Costa, Sueli M, Martins, Fábio Tadeu Arrojo, Pereira, Tânia, Pomilio, Mariza C A, Marques-de-Faria, Antonia Paula, Sartorato, Edi Lúcia

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Polycomb Repressive Complex 2 Regulates Genes Necessary for Intestinal Microfold Cell (M Cell) Development von George, Joel Johnson, Oittinen, Mikko, Martin-Diaz, Laura, Zapilko, Veronika, Iqbal, Sharif, Rintakangas, Terhi, Arrojo Martins, Fábio Tadeu, Niskanen, Henri, Katajisto, Pekka, Kaikkonen, Minna U., Viiri, Keijo

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Optimization of a genotyping screening based on hydrolysis probes to detect the main mutations related to Leber hereditary optic neuropathy (LHON) von Martins, Fábio Tadeu Arrojo, Miranda, Paulo Maurício do Amor Divino, Fernandes, Marcela Scabello Amaral, Maciel-Guerra, Andréa Trevas, Sartorato, Edi Lúcia

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Spectrum of genes for inherited hearing loss in the Israeli Jewish population, including the novel human deafness gene ATOH1 von Brownstein, Zippora, Gulsuner, Suleyman, Walsh, Tom, Martins, Fábio T.A., Taiber, Shahar, Isakov, Ofer, Lee, Ming K., Bordeynik‐Cohen, Mor, Birkan, Maria, Chang, Weise, Casadei, Silvia, Danial‐Farran, Nada, Abu‐Rayyan, Amal, Carlson, Ryan, Kamal, Lara, Arnthórsson, Asgeir Ö., Sokolov, Meirav, Gilony, Dror, Lipschitz, Noga, Frydman, Moshe, Davidov, Bella, Macarov, Michal, Sagi, Michal, Vinkler, Chana, Poran, Hana, Sharony, Reuven, Samra, Nadra, Zvi, Na'ama, Baris‐Feldman, Hagit, Singer, Amihood, Handzel, Ophir, Hertzano, Ronna, Ali‐Naffaa, Doaa, Ruhrman‐Shahar, Noa, Madgar, Ory, Sofrin‐Drucker, Efrat, Peleg, Amir, Khayat, Morad, Shohat, Mordechai, Basel‐Salmon, Lina, Pras, Elon, Lev, Dorit, Wolf, Michael, Steingrimsson, Eirikur, Shomron, Noam, Kelley, Matthew W., Kanaan, Moien N., Allon‐Shalev, Stavit, King, Mary‐Claire, Avraham, Karen B.

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Polycomb Repressive Complex 2 Regulates Genes Necessary for Intestinal Microfold Cell (M Cell) DevelopmentSummary von Joel Johnson George, Mikko Oittinen, Laura Martin-Diaz, Veronika Zapilko, Sharif Iqbal, Terhi Rintakangas, Fábio Tadeu Arrojo Martins, Henri Niskanen, Pekka Katajisto, Minna U. Kaikkonen, Keijo Viiri

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Optimization of simultaneous screening of the main mutations involved in non-syndromic deafness using the TaqMan registered OpenArray(TM) Genotyping Platform von Martins, Fabio Tadeu Arrojo, Ramos, Priscila Zonzini, Svidnicki, Maria Carolina Costa Melo, Castilho, Arthur Menino, Sartorato, Edi Lucia

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A rare case of deafness and renal abnormalities in HDR syndrome caused by a de novo mutation in the GATA3 gene von Fábio Tadeu Arrojo Martins, Ramos, Berenice Dias, Sartorato, Edi Lúcia

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A rare case of deafness and renal abnormalities in HDR syndrome caused by a de novo mutation in the GATA3 gene von Fábio Tadeu Arrojo Martins, Ramos, Berenice Dias, Sartorato, Edi Lúcia

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