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Your search keyword '"MacDowall, John"' showing total 14 results

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14 results on '"MacDowall, John"'

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1. Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

2. Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

3. Missense and truncating variants in CHD5 in a dominant neurodevelopmental disorder with intellectual disability, behavioral disturbances, and epilepsy

4. Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

5. Variants in PRKAR1B cause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

6. Correction to:An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids (Genetics in Medicine, (2021), 23, 4, (740-750), 10.1038/s41436-020-01027-3)

7. An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

8. Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science

9. Correction: Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

10. Variants in PRKAR1Bcause a neurodevelopmental disorder with autism spectrum disorder, apraxia, and insensitivity to pain

11. Commonalities across computational workflows for uncovering explanatory variants in undiagnosed cases

12. An autosomal dominant neurological disorder caused by de novo variants in FAR1resulting in uncontrolled synthesis of ether lipids

13. Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1resulting in uncontrolled synthesis of ether lipids

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