M. Lambert

De novo DNA microdeletion in a girl with Turner syndrome and Duchenne muscular dystrophy

Jamel Chelly, F. Marlhens, B. Le Marec et al. · Human Genetics · 1986 · 57 citations

Life Sciences, Genetics, Molecular Genetics +16

Illegitimate transcription. Application to the analysis of truncated transcripts of the dystrophin gene in nonmuscle cultured cells from Duchenne and Becker patients.

Jamel Chelly, Hélène Gilgenkrantz, Jean‐Philippe Hugnot et al. · Journal of Clinical Investigation · 1991 · 54 citations · Full text

Life Sciences, Genetics, Molecular Biology +14

Prenatal diagnosis of fetal anomalies during the second trimester of pregnancy: Their characterization and delineation of defects in pregnancies at risk

Louis Dallaire, Jacques L. Michaud, S.B. Melançon et al. · Prenatal Diagnosis · 1991 · 43 citations

Medicine, Genetics, Obstetrics +17

Positive and negative regulatory DNA elements including a CCArGG box are involved in the cell type-specific expression of the human muscle dystrophin gene.

Hélène Gilgenkrantz, Jean‐Philippe Hugnot, M. Lambert et al. · Journal of Biological Chemistry · 1992 · 36 citations · Full text

Life Sciences, Genetics, Molecular Biology +17

Analysis of molecular deletions with cDNA probes in patients with Duchenne and Becker muscular dystrophies

Hélène Gilgenkrantz, Jamel Chelly, M. Lambert et al. · Genomics · 1989 · 31 citations

Medicine, Genetics, Molecular Genetics +12