European Journal of Human Genetics Issues 16 Research Articles in July 2019 Edition
August 09, 2019
August 09, 2019
NEW YORK, Aug. 9 -- The European Journal of Human Genetics, a journal from the European Society of Human Genetics that focuses on human genetics and genomics, published 16 research articles on the following topics in its July 2019 edition:
* A novel dominant-negative FGFR1 variant causes Hartsfield syndrome by deregulating RAS/ERK1/2 pathway
* A novel variant of the human mitochondrial DnaJ protein, Tid1, associates with a human disease exhibiting developmental delay an . . .
* A novel dominant-negative FGFR1 variant causes Hartsfield syndrome by deregulating RAS/ERK1/2 pathway
* A novel variant of the human mitochondrial DnaJ protein, Tid1, associates with a human disease exhibiting developmental delay an . . .