Suchergebnisse - "Mighton, Chloe"

PubPharm (73)

1

Validation of low-pass genome sequencing for prenatal diagnosis

enthalten in: Prenatal diagnosis | 2024

von Mighton, C. | Noor, A. | Watkins, N. | +7

2

COVID-19 vaccine reactogenicity among participants enrolled in the GENCOV study

enthalten in: Vaccine | 2024

von Morgan, G. | Casalino, S. | Chowdhary, S. | +20

3

Parents' attitudes towards research involving genome sequencing of their healthy children : a qualitative study

enthalten in: European journal of human genetics : EJHG | 2024

von Di Carlo, C. | Mighton, C. | Clausen, M. | +7

4

"I don't need any more unknowns hanging over my head" : Views of patients with cancer on variants of uncertain significance and low/moderate risk results from genomic sequencing

enthalten in: Genetics in medicine : official journal of the American College of Medical Genetics | 2023

von Shickh, S. | Mighton, C. | Clausen, M. | +46

5

Certain heterozygous variants in the kinase domain of the serine/threonine kinase NEK8 can cause an autosomal dominant form of polycystic kidney disease

enthalten in: Kidney international | 2023

von Claus, L. | Chen, C. | Stallworth, J. | +102

6

Moving from intervention management to disease management : a qualitative study exploring a systems approach to health technology assessment in Canada

enthalten in: International journal of technology assessment in health care | 2023

von Richardson, M. | Sander, B. | Daneman, N. | +2

7

Public knowledge of SARS-CoV-2 serological and viral lineage laboratory testing and result interpretation : A GENCOV study cross-sectional survey

enthalten in: Clinical biochemistry | 2023

von Morgan, G. | Briollais, L. | Clausen, M. | +23

8

A model for the return and referral of all clinically significant secondary findings of genomic sequencing

enthalten in: Journal of medical genetics | 2023

von Kodida, R. | Reble, E. | Clausen, M. | +59

9

Loss-of-function variants inCUL3cause a syndromic neurodevelopmental disorder

enthalten in: bioRxiv.org | 2023

von Blackburn, P. | Ebstein, F. | Hsieh, T. | +72

10

Loss-of-function variants in CUL3 cause a syndromic neurodevelopmental disorder

enthalten in: medRxiv : the preprint server for health sciences | 2023

von Blackburn, P. | Ebstein, F. | Hsieh, T. | +72

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