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Acta Paediatrica Scandinavica|May 1, 1984
Immunoreactive copper-zinc superoxide-dismutase (SOD-1) in mosaic trisomy 21 and normal subjectsM A Baeteman, M G Mattei, A Baret, et al.Clinical Genetics|June 1, 1985
Clinical, chromosomal and enzymatic studies in four cases of rearrangements of chromosome 7M A Baeteman, N Philip, M G Mattei, et al.Human Genetics|January 1, 1983
Franceschetti syndrome in a child with a de novo balanced translocation (5;13)(q11;p11) and significant decrease of hexosaminidase BP Balestrazzi, M A Baeteman, M G Mattei, et al.Journal De Genetique Humaine|September 1, 1980
[Prenatal diagnosis of upper limb malformations]J F Mattei, J Cristofari, M Gamerre, 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.Genetic Counseling (Geneva, Switzerland)|January 1, 1992
Dysmorphology report: on the association of microcephaly and preaxial polydactyly. Another example of Howard-Young syndromeP Collignon, N Philip, G Simonin, et al.American Journal of Medical Genetics|January 1, 1982
GENTIC: a computerized medical genetic case record systemS Aymé, Y Aurran, J Gouvernet, et al.Clinical Genetics|January 1, 1979
Dermatoglyphics in parents of children with trisomy 21. Evaluation of their interest in genetic counsellingS Ayme, M G Mattei, J F Mattei, et al.Cytogenetics and Cell Genetics|January 1, 1979
Distribution of spontaneous chromosome breaks in manM G Mattei, S Ayme, J F Mattei, et al.Annales D'Endocrinologie|July 1, 1977
[46 XX karyotype men (author's transl)]J Vague, J Guidon, J F Mattei, et al.Pageof 14