Mapping of breakpoints in balanced chromosomal translocations by shallow whole-genome sequencing points to EFNA5, BAHD1 and PPP2R5E as novel candidates for genes causing human Mendelian disorders
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E. Obersztyn | R. Płoski | K. Chrzanowska | M. Rydzanicz | R. Śmigiel | P. Krajewski | Maciej Sykulski | A. Gambin | J. Kosińska | J. Castañeda | E. Jurkiewicz | R. Posmyk | K. Szczałuba | A. Skórka | M. Krajewska-Walasek | A. Walczak | A. Biernacka | M. Kucharczyk | Agnieszka Koppolu | Barbara Poszewiecka | Marlena Młynek | V. Murcia Pienkowski | Jennifer Castañeda