Publications
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Filters: Author is Karaca, Ender and Keyword is Genetic Diseases, Inborn [Clear All Filters]
Phenotypic expansion illuminates multilocus pathogenic variation. Genet Med. 2018 ;20(12):1528-1537.
. Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohort. Nucleic Acids Res. 2017 ;45(4):1633-1648.
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