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Publications by Peter D. Turnpenny
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
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
Recontacting Patients in Clinical Genetics Services: Recommendations of the European Society of Human Genetics
European Journal of Human Genetics
Genetics
Neonatal Lethal Costello Syndrome and Unusual Dinucleotide Deletion/Insertion Mutations in HRAS Predicting p.Gly12Val
American Journal of Medical Genetics, Part A
Genetics
Developing Diagnostic Criteria for the Fetal Anticonvulsant Syndromes
Seizure : the journal of the British Epilepsy Association
Medicine
Neurology
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Preexposure Prophylaxis for Prevention of HIV Acquisition Among Adolescents: Clinical Considerations, 2020
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Mutagenesis
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Sequencing Studies in Human Genetics: Design and Interpretation
Nature Reviews Genetics
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Evolution of Genetic and Genomic Features Unique to the Human Lineage
Nature Reviews Genetics
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Recent Human Adaptation: Genomic Approaches, Interpretation and Insights
Nature Reviews Genetics
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ChIP–seq and Beyond: New and Improved Methodologies to Detect and Characterize Protein–DNA Interactions
Nature Reviews Genetics
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Molecular Biology
Sex and the Singular DM Domain: Insights Into Sexual Regulation, Evolution and Plasticity
Nature Reviews Genetics
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Putting Gene Essentiality Into Context
Nature Reviews Genetics
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Promoter-Proximal Pausing of RNA Polymerase II: Emerging Roles in Metazoans
Nature Reviews Genetics
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Stress and the Epigenetic Landscape: A Link to the Pathobiology of Human Diseases?
Nature Reviews Genetics
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