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1. Experience of the first adult-focussed undiagnosed disease program in Australia (AHA-UDP): solving rare and puzzling genetic disorders is ageless

2. An iPSC line (FINi003-A) from a male with late-onset developmental and epileptic encephalopathy caused by a heterozygous p.E1211K variant in the SCN2A gene encoding the voltage-gated sodium channel Nav1.2

6. Primary Results Of The REVEALPLAQUE Study: A Prospective Quantitative Assessment Of AI-based CCTA Plaque Volume Compared With IVUS

9. Properties of Rubble-Pile Asteroid (101955) Bennu from OSIRIS-REx Imaging and Thermal Analysis

10. Changing the culture: a qualitative study exploring research capacity in local government

13. Borgs are giant extrachromosomal elements with the potential to augment methane oxidation

15. Craters, boulders and regolith of (101955) Bennu indicative of an old and dynamic surface

16. Somatic IDH1 variant ( p.R132C) in an adult male with Maffucci syndrome

19. 1-Year Impact on Medical Practice and Clinical Outcomes of FFRCT:The ADVANCE Registry

20. Inherited RORB pathogenic variants: Overlap of photosensitive genetic generalized and occipital lobe epilepsy

23. Hybridization and speciation*

30. Evidence for widespread hydrated minerals on asteroid (101955) Bennu

31. The dynamic geophysical environment of (101955) Bennu based on OSIRIS-REx measurements

33. The operational environment and rotational acceleration of asteroid (101955) Bennu from OSIRIS-REx observations

34. Design and Implementation of the Hangman Gbit/S Network

38. Real-world clinical utility and impact on clinical decision-making of coronary computed tomography angiography-derived fractional flow reserve: lessons from the ADVANCE Registry

39. Real-world clinical utility and impact on clinical decision-making of coronary computed tomography angiography-derived fractional flow reserve: lessons from the ADVANCE Registry

43. Spin-on metal oxide materials for N7 and beyond patterning applications

45. Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies

46. Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies

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