Mapping of breakpoints in balanced chromosomal translocations by shallow whole-genome sequencing points to , and as novel candidates for genes causing human Mendelian disorders
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author: Victor Murcia Pienkowski, Marlena Mlynek, Krzysztof Szczałuba, Agnieszka Koppolu, Anna Gambin, Krystyna Chrzanowska, Małgorzata Krajewska-Walasek, Rafał Płoski, Robert Śmigiel, Małgorzata Rydzanicz, Paweł Krajewski, Agata Skórka, Ewa Obersztyn, Marzena Kucharczyk, Renata Posmyk, Barbara Poszewiecka, Jennifer Castaneda
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