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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: Małgorzata Rydzanicz  Victor Murcia Pienkowski  Agnieszka Koppolu  Barbara Poszewiecka  Renata Posmyk  Małgorzata Krajewska-Walasek  Paweł Krajewski  Jennifer Castaneda  Marzena Kucharczyk  Krystyna Chrzanowska  Agata Skórka  Robert Smigiel  Anna Gambin  Krzysztof Szczałuba  Ewa Obersztyn  Rafał Płoski  Marlena Mlynek 

Publication date October 23, 2018
Language English
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