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3. Biallelic CRELD1 variants cause a multisystem syndrome including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.

9. Estuarine movements in a sparid hybrid complex

11. Detailed benchmarking of the Nernst effect in magnetized HED plasma.

21. Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

23. One is the loneliest number: genotypic matchmaking using the electronic health record

24. Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

29. An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids

30. Clinical sites of the Undiagnosed Diseases Network: unique contributions to genomic medicine and science

32. Mesenchymal Stem/Stromal Cells Increase Cardiac MIR-187-3P Expression in Polymicrobial Animal Model of Sepsis

37. De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic Decompensation

38. Palliative Care Transitions from Acute Care to Community-Based Care—A Systematic Review (FR420A)

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

50. Magnetic Resonance Imaging characteristics in case of TOR1AIP1 muscular dystrophy

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