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1. An HNRNPK-specific DNA methylation signature makes sense of missense variants and expands the phenotypic spectrum of Au-Kline syndrome

2. Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology

5. A dyadic approach to the delineation of diagnostic entities in clinical genomics

7. GATAD2B-associatedneurodevelopmental disorder (GAND): clinical and molecular insights into a NuRD-relateddisorder

8. Partial Loss of USP9X Function Leads to a Male Neurodevelopmental and Behavioral Disorder Converging on Transforming Growth Factor β Signaling

10. De novo and biallelic DEAF1 variants cause a phenotypic spectrum

11. Variants in TCF20 in neurodevelopmental disability: description of 27 new patients and review of literature

12. Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons

13. IRF2BPL Is Associated with Neurological Phenotypes

17. Radial versus femoral access for percutaneous coronary intervention in ST-elevation myocardial infarction patients treated with fibrinolysis: Results from the randomized routine early invasive clinical trials

26. Variants in PHF8 cause a spectrum of X-linked neurodevelopmental disorders and facial dysmorphology

28. Management and Outcomes of Non-ST Elevation Acute Coronary Syndromes in Relation to Previous Use of Antianginal Therapies (from the Canadian Global Registry of Acute Coronary Events [GRACE] and Canadian Registry of Acute Coronary Events [CANRACE])

38. SPEN haploinsufficiency causes a neurodevelopmental disorder overlapping proximal 1p36 deletion syndrome with an episignature of X chromosomes in females

45. Spectrum of CHD7 Mutations in 110 Individuals with CHARGE Syndrome and Genotype-Phenotype Correlation

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