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Genetical Research|June 1, 1989
Chromosomal localization of the mouse gene coding for vimentinM G Mattei, A Lilienbaum, L Z Lin, et al.
Genetical Research|April 1, 1990
Assignment of the mouse desmin gene to chromosome 1 band C3Z L Li, M G Mattei, J F Mattei, et al.
Biology of the Cell|January 1, 1989
Chromosomal localization of the mouse gene coding for the 68 kDa neurofilament subunitM G Mattei, P Duprey, Z L Li, et al.
Annales De Genetique|September 1, 1977
[Partial trisomy 13 due to maternal translocation t(2;13)]F Giraud, J F Mattei, M G Mattei
Human Genetics|January 1, 1984
Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysisM G Mattei, N Souiah, J F Mattei
Human Genetics|January 1, 1983
Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 casesJ F Mattei, M G Mattei, F Giraud
Archives Francaises De Pediatrie|August 1, 1985
[Contribution of in situ hybridization to chromosomal analysis]M G Mattei, J F Mattei, F Giraud
Journal of Submicroscopic Cytology and Pathology|January 1, 1990
Expression of desmin gene in skeletal and smooth muscle by in situ hybridization using a human desmin gene probeC Bolmont, A Lilienbaum, D Paulin, et al.
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