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You searched for: Author/Creator Bonner Devon investigator.

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1. Clinical application of a scale to assess genomic healthcare empowerment (GEmS): Process and illustrative case examples. Issue 1 (11th June 2021)

2. Detection of a mosaic CDKL5 deletion and inversion by optical genome mapping ends an exhaustive diagnostic odyssey. Issue 7 (6th May 2021)

3. Developing a genomics rotation: Practical training around variant interpretation for genetic counseling students. Issue 2 (1st February 2019)

4. DYRK1A pathogenic variants in two patients with syndromic intellectual disability and a review of the literature. Issue 12 (7th November 2020)

5. Early infantile epileptic encephalopathy due to biallelic pathogenic variants in PIGQ: Report of seven new subjects and review of the literature. Issue 6 (3rd August 2020)

6. Family genetic result communication in rare and undiagnosed disease communities: Understanding the practice. Issue 2 (27th October 2020)

7. Genetic counselor roles in the undiagnosed diseases network research study: Clinical care, collaboration, and curation. Issue 2 (10th August 2021)

8. Genome sequencing reveals novel noncoding variants in PLA2G6 and LMNB1 causing progressive neurologic disease. Issue 4 (5th March 2022)

9. Heterozygous variants in MYBPC1 are associated with an expanded neuromuscular phenotype beyond arthrogryposis. Issue 8 (5th May 2019)

10. IgG4‐related disease: Association with a rare gene variant expressed in cytotoxic T cells. Issue 6 (16th April 2019)