Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by L Colvin
Refining the Phenotype of Common Mutations in Rett Syndrome
Journal of Medical Genetics
Genetics
Related publications
MeCP2 Mutations in Children With and Without the Phenotype of Rett Syndrome
Neurology
Neurology
Genotype-Phenotype Correlation in Brazillian Rett Syndrome Patients
Arquivos de Neuro-Psiquiatria
Biological Psychiatry
Neurology
MECP2 Mutations Associated With Rett Syndrome - Molecular Approaches
Journal of Neonatal Biology
Rett Syndrome.
Journal of Medical Genetics
Genetics
Atypical Rett Syndrome
Specific Mutations in Methyl-CpG-Binding Protein 2 Confer Different Severity in Rett Syndrome
Neurology
Neurology
Rett Syndrome and MeCP2
NeuroMolecular Medicine
Molecular Neuroscience
Neurology
Molecular Medicine
Cellular
The American History of Rett Syndrome
Pediatric Neurology
Child Health
Developmental Neuroscience
Pediatrics
Perinatology
Neurology
Microvascular Abnormalities in Rett Syndrome
Clinical Hemorheology and Microcirculation
Physiology
Cardiovascular Medicine
Hematology
Cardiology