Novel mutation in the CHST6 gene causes macular corneal dystrophy in a black South African family

por Carstens, Nadia, Williams, Susan, Goolam, Saadiah, Carmichael, Trevor, Cheung, Ming Sin, Büchmann-Møller, Stine, Sultan, Marc, Staedtler, Frank, Zou, Chao, Swart, Peter, Rice, Dennis S., Lacoste, Arnaud, Paes, Kim, Ramsay, Michèle
Publicado 2016

Heart Structure-Specific Transcriptomic Atlas Reveals Conserved microRNA-mRNA Interactions

por Vacchi-Suzzi, Caterina, Hahne, Florian, Scheubel, Philippe, Marcellin, Magali, Dubost, Valerie, Westphal, Magdalena, Boeglen, Catherine, Büchmann-Møller, Stine, Cheung, Ming Sin, Cordier, André, De Benedetto, Christopher, Deurinck, Mark, Frei, Moritz, Moulin, Pierre, Oakeley, Edward, Grenet, Olivier, Grevot, Armelle, Stull, Robert, Theil, Diethilde, Moggs, Jonathan G., Marrer, Estelle, Couttet, Philippe
Publicado 2013

What is the right sequencing approach? Solo VS extended family analysis in consanguineous populations

por Alfares, Ahmed, Alsubaie, Lamia, Aloraini, Taghrid, Alaskar, Aljoharah, Althagafi, Azza, Alahmad, Ahmed, Rashid, Mamoon, Alswaid, Abdulrahman, Alothaim, Ali, Eyaid, Wafaa, Ababneh, Faroug, Albalwi, Mohammed, Alotaibi, Raniah, Almutairi, Mashael, Altharawi, Nouf, Alsamer, Alhanouf, Abdelhakim, Marwa, Kafkas, Senay, Mineta, Katsuhiko, Cheung, Nicole, Abdallah, Abdallah, Büchmann-Møller, Stine, Fukasawa, Yoshinori, Zhao, Xiang, Rajan, Issaac, Hoehndorf, Robert, Al Mutairi, Fuad, Gojobori, Takashi, Alfadhel, Majid
Publicado 2020