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You searched for: Author/Creator Lau C. Christopher investigator.

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1. A toolkit for genetics providers in follow‐up of patients with non‐diagnostic exome sequencing. Issue 2 (9th April 2019)

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

3. 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)

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

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

6. 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)

7. Spectrum of neurodevelopmental disease associated with the GNAO1 guanosine triphosphate–binding region. (25th January 2019)

8. Whole genome sequencing reveals novel IGHMBP2 variant leading to unique cryptic splice‐site and Charcot‐Marie‐Tooth phenotype with early onset symptoms. Issue 6 (25th April 2019)