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203 ELN Gene: UKGTN Service for SVAS and Cutis Laxa. Copy Number Variants (CNVS) Are a Common Cause of Disease
by Gable, Mary
Heart (British Cardiac Society), 2016-06, Vol.102 (Suppl 6), p.A135-A136
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210 Clinical Utility of Gene Panel and Clinical Exome Testing in Cardiac Disease
by Gable, Mary
Heart (British Cardiac Society), 2016-06, Vol.102 (Suppl 6), p.A139-A140
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196 Paediatric Cardiomyopathy (PC); The Validation, Implementation and Utility of a 71 Gene NGS Diagnostic Panel to Detect Variants in Rare Cardiac Genes
by Gable, Mary
Heart (British Cardiac Society), 2015-06, Vol.101 (Suppl 4), p.A109-A109
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196Paediatric Cardiomyopathy (PC); The Validation, Implementation and Utility of a 71 Gene NGS Diagnostic Panel to Detect Variants in Rare Cardiac Genes
by Gable, Mary
Heart (British Cardiac Society), 2015-06-01, Vol.101 (Suppl 4), p.A109-A109
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A Syndromic Intellectual Disability Disorder Caused by Variants in TELO2, a Gene Encoding a Component of the TTT Complex
by You, Jing
American journal of human genetics, 2016-05-05, Vol.98 (5), p.909-918
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Predictors of epinephrine autoinjector needle length inadequacy
by Bhalla, Mary Colleen, MD
The American journal of emergency medicine, 2013, Vol.31 (12), p.1671-1676
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Global and regional mortality from 235 causes of death for 20 age groups in 1990 and 2010: a systematic analysis for the Global Burden of Disease Study 2010
by Lozano, Rafael, Prof
The Lancet (British edition), 2012, Vol.380 (9859), p.2095-2128
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Clinical Pharmacist Interventions on an Assertive Community Treatment Team
by Gable, Kelly N
Community mental health journal, 2009-10-07, Vol.46 (4), p.351-355
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Heritage characteristics reported by a group of African-Americans who exhibit the pigment dispersion syndrome : a case-control study
by ROBERTS, Daniel K
Documenta ophthalmologica, 2000, Vol.101 (3), p.179-193
