Showing results 1 to 4 of 4
Title | Author(s) | Issue Date | |
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Cost effective assay choice for rare disease study designs Proceeding/Conference:Human Heredity | 2015 | ||
Cost effective assay choice for rare disease study designs Journal:Orphanet Journal of Rare Diseases | 2015 | ||
De novo mutations associated with sporadic cases of Caudal regresion syndrome Proceeding/Conference:European Journal of Human Genetics | 2014 | ||
Sacral agenesis: a pilot whole exome sequencing and copy number study Journal:BMC Medical Genetics | 2016 |