Richard J. Allcock
Nedlands, WA, Australia
Last Updated: 09/26/2026
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Found 9 publications
Platelets in myeloproliferative neoplasms have a distinct transcript signature in the presence of marrow fibrosis.
Journal: British journal of haematology
Published: April 08, 2019
Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes.
Journal: Journal of hypertension
Published: January 12, 2019
Megakaryocytes in Myeloproliferative Neoplasms Have Unique Somatic Mutations.
Journal: The American journal of pathology
Published: February 10, 2017
Mutations of GPR126 are responsible for severe arthrogryposis multiplex congenita.
Journal: American journal of human genetics
Published: February 13, 2015
Novel CHKB mutation expands the megaconial muscular dystrophy phenotype.
Journal: Muscle & nerve
Published: August 29, 2014
Novel cofilin-2 (CFL2) four base pair deletion causing nemaline myopathy.
Journal: Journal of neurology, neurosurgery, and psychiatry
Published: March 11, 2014
Detection of variations and identifying genomic breakpoints for large deletions in the LDLR by Ion Torrent semiconductor sequencing.
Journal: Atherosclerosis
Published: June 26, 2013
Whole exome sequencing in foetal akinesia expands the genotype-phenotype spectrum of GBE1 glycogen storage disease mutations.
Journal: Neuromuscular disorders : NMD
Published: June 07, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026