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Dewi S. Clark
Dewi S. Clark
St. Michael's Hospital
ACVRL1
Telangiectasia
Genotype
Medicine
Mutation
4
Papers
42
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Reduction of endoglin receptor impairs mononuclear cell-migration
2020
Zhenying Han
Sonali Shaligram
Marie E. Faughnan
Dewi S. Clark
Zhengda Sun
Hua Su
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Citations (2)
Genotype-Phenotype Correlations in Children with HHT.
2020
Journal of Clinical Medicine
Alexandra Kilian
Giuseppe A Latino
Andrew J. White
Dewi S. Clark
Murali M. Chakinala
Felix Ratjen
Jamie McDonald
Kevin J. Whitehead
James R. Gossage
Doris D.M. Lin
Katharine J. Henderson
Jeffrey Pollak
Justin P. McWilliams
Helen Kim
Michael T. Lawton
Marie E. Faughnan
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Citations (3)
Somatic Mutations in Vascular Malformations of Hereditary Hemorrhagic Telangiectasia Result in Biallelic Loss of ENG or ACVRL1
2019
bioRxiv
Daniel A. Snellings
Carol J. Gallione
Dewi S. Clark
Nicholas T. Vozoris
Marie E. Faughnan
Douglas A. Marchuk
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Citations (2)
Somatic Mutations in Vascular Malformations of Hereditary Hemorrhagic Telangiectasia Result in Bi-allelic Loss of ENG or ACVRL1
2019
American Journal of Human Genetics
Daniel A. Snellings
Carol J. Gallione
Dewi S. Clark
Nicholas T. Vozoris
Marie E. Faughnan
Douglas A. Marchuk
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Citations (35)
1