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Publications in Genetics
This Month in the Journal
American Journal of Human Genetics
Genetics
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated With Craniofacial, Neurological, Cardiovascular, and Skeletal Features
American Journal of Human Genetics
Genetics
Lessons Learned From Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population
American Journal of Human Genetics
Genetics
De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A (PPP2CA) Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders
American Journal of Human Genetics
Genetics
Monitoring Protein Conformational Changes and Dynamics Using Stable-Isotope Labeling and Mass Spectrometry
Nature Protocols
Biochemistry
Genetics
Molecular Biology
Genetic Basis of Y-Linked Hearing Impairment
American Journal of Human Genetics
Genetics
This Month in the Journal
American Journal of Human Genetics
Genetics
PSMB8 Encoding the Β5i Proteasome Subunit Is Mutated in Joint Contractures, Muscle Atrophy, Microcytic Anemia, and Panniculitis-Induced Lipodystrophy Syndrome
American Journal of Human Genetics
Genetics
The Biology of Cell-Free DNA Fragmentation and the Roles of DNASE1, DNASE1L3, and DFFB
American Journal of Human Genetics
Genetics
Single-mRNA Counting Using Fluorescent in Situ Hybridization in Budding Yeast
Nature Protocols
Biochemistry
Genetics
Molecular Biology
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