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European Journal of Human Genetics, ISSN 1018-4813, 02/2019, Volume 27, Issue 2, pp. 325 - 330
Clinical genomic sequencing can identify pathogenic variants unrelated to the initial clinical question, but of medical relevance to the patients and their... 
INCIDENTAL FINDINGS | RECOMMENDATIONS | GENETICS | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | AMERICAN-COLLEGE | SECONDARY FINDINGS | SEQUENCE VARIANTS | CLINICAL EXOME | Cost-benefit analysis | Gene frequency | Genomics | Alleles | Data processing | Health risk assessment | Population genetics | Index Medicus
Journal Article
Nature Genetics, ISSN 1061-4036, 11/2015, Volume 47, Issue 11, pp. 1222 - 1224
Journal Article
Journal Article
Nature Reviews Genetics, ISSN 1471-0056, 01/2016, Volume 17, Issue 1, pp. 9 - 18
Journal Article
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 10, pp. 1063 - 1071
Journal Article
Cell, ISSN 0092-8674, 09/2014, Volume 159, Issue 1, pp. 200 - 214
Journal Article
Cell, ISSN 0092-8674, 07/2014, Volume 158, Issue 2, pp. 263 - 276
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 08/2014, Volume 95, Issue 2, pp. 173 - 182
Journal Article
Nature Genetics, ISSN 1061-4036, 2010, Volume 42, Issue 12, pp. 1109 - 1112
The per-generation mutation rate in humans is high. De novo mutations may compensate for allele loss due to severely reduced fecundity in common... 
MICE | MUTATIONS | GENE | DYNEIN | GENETICS & HEREDITY | Base Sequence | Humans | Exons - genetics | Female | Male | Mutation - genetics | Sequence Analysis, DNA | Intellectual Disability - genetics | Genetic aspects | Research | Gene mutations | Health aspects | Mental retardation | Risk factors | Studies | Candidates | Disease | Genetics | Mutation | Experiments | Chromosomes | Index Medicus
Journal Article
Nature Genetics, ISSN 1061-4036, 2014, Volume 46, Issue 4, pp. 380 - 384
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 07/2012, Volume 91, Issue 1, pp. 73 - 82
Journal Article