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Why My Baby's Blindness Diagnosis Inspired Me to Keep Working and Start a Business

Why My Baby’s Blindness Diagnosis Inspired Me to Keep Working and Start a Business

Editor’s note: In 2021, Leslie Danford launched her business while pregnant with her fourth child. After failing his newborn hearing screening, the Danford infant was later diagnosed with Usher Syndrome Type 1B, a rare genetic condition that impairs hearing, balance and will likely lead to loss of vision in childhood. Although there is no cure …

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Dutch Pharmacogenetics Working Group (DPWG) Guidelines for Gene-Drug Interaction Between UGT1A1 and Irinotecan – European Journal of Human Genetics

Swen J, Wilting I, Goede A, de, Grandia L, Mulder H, Touw D, and others Pharmacogenetics: From Bench to Byte. Clin Pharm Ther. 2008;83:781–7. https://doi.org/10.1038/sj.clpt.6100507. Google Scholar article Guchelaar HJ. Pharmacogenomics, a new section of the European Journal of Human Genetics. Eur J Hum Genet. 2018;26:1399–400. https://doi.org/10.1038/s41431-018-0205-4. PubMed Article PubMed Central Google Scholar Lunenburg CATC, …

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