Michel Bahuau
Creteil, France
Last Updated: 09/26/2026
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Found 9 publications
Methylation-sensitive high-resolution melting technology is a simple and sensitive method to detect germline epimutation of the MLH1 gene promoter.
Journal: Clinical epigenetics
Published: March 24, 2025
Biochemical screening of glucose-6-phosphate dehydrogenase deficiency in borderline cases: Complementary inputs of standardization enzymes and comparison with genetic status.
Journal: British journal of haematology
Published: September 29, 2024
MSH3: a confirmed predisposing gene for adenomatous polyposis.
Journal: Journal of medical genetics
Published: April 25, 2023
Further delineation of the NTHL1 associated syndrome: A report from the French Oncogenetic Consortium.
Journal: Clinical genetics
Published: November 04, 2020
Exome sequencing for diagnosis of congenital hemolytic anemia.
Journal: Orphanet journal of rare diseases
Published: February 20, 2020
Pyrimidine 5'-nucleotidase deficiency associated to a polymalformative syndrome.
Journal: Annales de biologie clinique
Published: October 23, 2015
Exercise-induced muscle pain due to phosphofrutokinase deficiency: Diagnostic contribution of metabolic explorations (exercise tests, 31P-nuclear magnetic resonance spectroscopy)
Journal: Revue neurologique
Published: February 16, 2012
Practical approach for characterization of glucose 6-phosphate dehydrogenase (G6PD) deficiency in countries with population ethnically heterogeneous: description of seven new G6PD mutants.
Journal: American journal of hematology
Published: September 30, 2011
Showing 1-9 of 9
Last Updated: 09/26/2026