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

4. 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)

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

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

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

8. Progressive cerebellar atrophy in a patient with complex II and III deficiency and a novel deleterious variant in SDHA: A Counseling Conundrum. Issue 6 (7th May 2021)

9. Whole genome sequencing of Caribbean Hispanic families with late‐onset Alzheimer's disease. Issue 4 (13th March 2018)