Associated Papers
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Supplement: 40246_2022_402_MOESM5_ESM.xlsx › Additional_File_5
Whole exome sequencing identified mutations causing hearing loss in five consanguineous Pakistani families.
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Bmc Medical Genetics, 2020
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Results of genetic testing in 855 consecutive unrelated patients referred for long QT syndrome in a clinical laboratory.
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Supplement: sj-doc-1-gtm-10.1089_gtmb.2012.0118.doc
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