Search

Search Constraints

You searched for: Author/Creator Miller, David T.

Search Results

2. BRAT1 mutations present with a spectrum of clinical severity. Issue 9 (9th June 2016)

4. Clinical Trial of the Protein Farnesylation Inhibitors Lonafarnib, Pravastatin, and Zoledronic Acid in Children With Hutchinson-Gilford Progeria Syndrome. Issue 2 (12th July 2016)

6. Copy number variation plays an important role in clinical epilepsy. Issue 6 (13th June 2014)

7. GenomeConnect: Matchmaking Between Patients, Clinical Laboratories, and Researchers to Improve Genomic Knowledge. Issue 10 (6th August 2015)

8. Growth, development, and phenotypic spectrum of individuals with deletions of 2q33.1 involving SATB2. Issue 4 (13th January 2021)