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Publications by Noelle Lachaussée
Correction: A Homozygous KAT2B Variant Modulates the Clinical Phenotype of ADD3 Deficiency in Humans and Flies
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
Related publications
A New Family With a Homozygous Nonsense Variant in NTHL1 Further Delineated the Clinical Phenotype of NTHL1-associated Polyposis
Human Genome Variation
Biochemistry
Genetics
Molecular Biology
PNPO Deficiency and Cirrhosis: Expanding the Clinical Phenotype?
JIMD Reports
Internal Medicine
Genetics
Molecular Biology
Biochemistry
Endocrinology
Metabolism
Diabetes
The PNPLA3 I148M Variant Modulates the Fibrogenic Phenotype of Human Hepatic Stellate Cells
Hepatology
Medicine
Hepatology
Phenotype and Genotype Report on Homozygous and Heterozygous Patients With Congenital Factor X Deficiency
Haematologica
Hematology
SAT0597 New Autoinflammatory Phenotype Manifesting as Hypocomplementemic Urticarial Vasculitis and Associated With Homozygous Agbl3 Variant
Histamine Transmission Modulates the Phenotype of Murine Narcolepsy Caused by Orexin Neuron Deficiency
PLoS ONE
Multidisciplinary
The Enamel Phenotype in Homozygous Fam83h Truncation Mice
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Pupation in Mycetophilid Flies: A Correction
Psyche (New York)
Insect Science
Evolution
Ecology
Systematics
Behavior
Effects of Homozygous Apolipoprotein A-1 Deficiency on the Cornea
British Journal of Ophthalmology
Molecular Neuroscience
Ophthalmology
Sensory Systems
Cellular