Devon R. Mcleod
Calgary, AB T2N4N1, Canada
Last Updated: 09/26/2026
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Found 13 publications
Clinical and molecular characterization of an almost complete ring chromosome 4 in two sisters, with recurrence due to gonadal mosaicism.
Journal: Clinical dysmorphology
Published: August 21, 2021
An online Sexual Health and Rehabilitation eClinic (TrueNTH SHAReClinic) for prostate cancer patients: a feasibility study.
Journal: Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer
Published: April 23, 2021
Expanding the genotypic and phenotypic spectrum in a diverse cohort of 104 individuals with Wiedemann-Steiner syndrome.
Journal: American journal of medical genetics. Part A
Published: September 28, 2020
Number of Brain States in an N-Body Dynamical Scenario According to the Universal Bekenstein Entropy Bound.
Journal: Advances in experimental medicine and biology
Published: May 30, 2020
Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8.
Journal: American journal of human genetics
Published: July 08, 2015
Matching two independent cohorts validates DPH1 as a gene responsible for autosomal recessive intellectual disability with short stature, craniofacial, and ectodermal anomalies.
Journal: Human mutation
Published: May 06, 2015
Disrupted auto-regulation of the spliceosomal gene SNRPB causes cerebro-costo-mandibular syndrome.
Journal: Nature communications
Published: February 07, 2014
Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability.
Journal: American journal of human genetics
Published: March 19, 2013
Intellectual disability associated with a homozygous missense mutation in THOC6.
Journal: Orphanet journal of rare diseases
Published: February 12, 2013
Dental abnormalities in Schimke immuno-osseous dysplasia.
Journal: Journal of dental research
Published: June 16, 2012
Infantile ictal apneas in a child with williams-beuren syndrome.
Journal: Pediatric neurology
Published: May 19, 2012
Reduced elastogenesis: a clue to the arteriosclerosis and emphysematous changes in Schimke immuno-osseous dysplasia?
Journal: Orphanet journal of rare diseases
Published: March 15, 2012
Last Updated: 09/26/2026