M. A. Baeteman

Trisomy 21 for the region 21q223: Identification by high-resolution R-banding patterns

J. F. Mattéi, Marie‐Geneviève Mattéi, M. A. Baeteman et al. · Human Genetics · 1981 · 47 citations

Region 21Q223, Cytogenetics, High-resolution R-banding Patterns +11

Immunoreactive Cu SOD and Mn SOD in the circulating blood cells from normal and trisomy 21 subjects

A Baret, M. A. Baeteman, J. F. Mattéi et al. · Biochemical and Biophysical Research Communications · 1981 · 42 citations

Autoimmune Disease, Allergy, Immunology +8

Localization by in situ hybridization of the coagulation factor IX gene and of two polymorphic DNA probes with respect to the fragile X site

Marie‐Geneviève Mattéi, M. A. Baeteman, Roland Heilig et al. · Human Genetics · 1985 · 41 citations

Fragile X Site, Chromatin, Cytogenetics +15

Franceschetti syndrome in a child with a de novo balanced translocation (5;13)(q11;p11) and significant decrease of hexosaminidase B

P Balestrazzi, M. A. Baeteman, Marie‐Geneviève Mattéi et al. · Human Genetics · 1983 · 39 citations

Mendelian Disorder, Hexosaminidase B, Franceschetti Syndrome +6

ERYTHROCYTE SUPEROXIDE DISMUTASE AND REDOX ENZYMES IN TRISOMY 21

J. F. Mattéi, M. A. Baeteman, A Baret et al. · Acta Paediatrica · 1982 · 23 citations

Biochemistry, Genetics, Hematology +9