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Publications by M-P Cordier
New Ocular Phenotype Associated With a Mutation in the PAX2 Gene
Eye
Medicine
Arts
Sensory Systems
Ophthalmology
Humanities
Related publications
A Common Variant of the PAX2 Gene Is Associated With Reduced Newborn Kidney Size
Journal of the American Society of Nephrology : JASN
Medicine
Nephrology
Correction: A Unique Mutation in a MYB Gene Cosegregates With the Nectarine Phenotype in Peach
PLoS ONE
Multidisciplinary
A Single-Nucleotide Mutation in a Gene Encoding S-Adenosylmethionine Synthetase Is Associated With Methionine Over-Accumulation Phenotype in Arabidopsis Thaliana
Genes and Genetic Systems
Medicine
Genetics
Molecular Biology
Systematic Review of Kabuki Syndrome’s Phenotype With KMT2D Gene Mutation
Revista Intertox de Toxicologia, Risco Ambiental e Sociedade
A New Complex Allele of the CFTR Gene Partially Explains the Variable Phenotype of the L997F Mutation
Genetics in Medicine
Medicine
Genetics
Novel Epilepsy Phenotype Associated to a Known SCN8A Mutation
Seizure : the journal of the British Epilepsy Association
Medicine
Neurology
Identification and Validation of Mutation Points Associated With Waxy Phenotype in Cassava
BMC Plant Biology
Plant Science
Does the Timing of Treatment Affect the Ocular Phenotype in Patients With Mucopolysaccharidosis I Homozygous for the L490P Mutation?
Eye
Medicine
Arts
Sensory Systems
Ophthalmology
Humanities
A Nonsense Mutation (E1978X) in the ATM Gene Is Associated With Breast Cancer
Breast Cancer Research and Treatment
Cancer Research
Oncology
