Found: 7
Select item for more details and to access through your institution.
Heterozygous and Homozygous Variants in SORL1 Gene in Alzheimer's Disease Patients: Clinical, Neuroimaging and Neuropathological Findings.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 8, p. 4230, doi. 10.3390/ijms23084230
- By:
- Publication type:
- Article
First patient with mosaic NOTCH3 gene pathogenic variant. Unrevealed mosaicisms and importance of their detection.
- Published in:
- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 2, p. 591, doi. 10.1002/ajmg.a.61999
- By:
- Publication type:
- Article
Fragile X Syndrome Caused by Maternal Somatic Mosaicism of FMR1 Gene: Case Report and Literature Review.
- Published in:
- 2022
- By:
- Publication type:
- Case Study
Towards a Change in the Diagnostic Algorithm of Autism Spectrum Disorders: Evidence Supporting Whole Exome Sequencing as a First-Tier Test.
- Published in:
- Genes, 2021, v. 12, n. 4, p. 560, doi. 10.3390/genes12040560
- By:
- Publication type:
- Article
Superconductivity in Graphene: Observation of Yu–Shiba–Rusinov States in Superconducting Graphene (Adv. Mater. 22/2021).
- Published in:
- Advanced Materials, 2021, v. 33, n. 22, p. 1, doi. 10.1002/adma.202008113
- By:
- Publication type:
- Article
Observation of Yu–Shiba–Rusinov States in Superconducting Graphene.
- Published in:
- Advanced Materials, 2021, v. 33, n. 22, p. 1, doi. 10.1002/adma.202008113
- By:
- Publication type:
- Article
Quantum Confinement of Dirac Quasiparticles in Graphene Patterned with Sub‐Nanometer Precision.
- Published in:
- Advanced Materials, 2020, v. 32, n. 30, p. 1, doi. 10.1002/adma.202001119
- By:
- Publication type:
- Article