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J-F Mattei

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Biochemical and Biophysical Research Communications|February 27, 1981
Immunoreactive Cu SOD and Mn SOD in the circulating blood cells from normal and trisomy 21 subjectsA Baret, M A Baeteman, J F Mattei, et al.
Hemoglobin|September 8, 1998
A novel polymorphism 3' to the beta-globin geneC Badens, T Merghoub, D Lena-Russo, et al.
Pediatrie|January 1, 1978
[Neuroleptic poisoning in childhood]G Bosvieux, M C Galland, C Tomasi, et al.
Annales De Genetique|January 1, 1989
[Diagnosis of minor chromosome modifications by molecular cytogenetics]S Taviaux, A Moncla, F Giraud, et al.
Journal De Genetique Humaine|November 1, 1976
[The diminished forms of ectroprosopia: case report with unilateral proboscis]F Giraud, H Bureau, J B Saracco, et al.
Human Genetics|January 1, 1981
Morquio syndrome: clinical findings in 11 patients with MPS IVA and 2 patients with MPS IVBW Holzgreve, H Gröbe, K von Figura, et al.
Journal De Genetique Humaine|December 1, 1981
[Association, in the same subject, of deletion of the short arm of chromosome 4 (4p-) and of complete deficiency of parahydroxyphenyl-pyruvate oxidase activity in the liver (tyrosinosis)]G Malpuech, J F Mattei, J Gaulme, et al.
Marseille Medical|January 1, 1971
[Clinical, mitotic and meiotic study of a trisomy 21 with diabetes in a 52 year old man]F Giraud, J M Luciani, J F Mattei, et al.
Journal of Mental Deficiency Research|September 1, 1979
Erythrocyte copper levels in children with trisomy 21B Mallet, P Poulet, S Ayme, et al.
Human Genetics|January 1, 1987
Monosomy 21: a new case confirmed by in situ hybridizationM C Pellissier, N Philip, M A Voelckel-Baeteman, et al.
Pageof 21

Showing results (131-140 of 202) with videos related to

Sort By:
Pageof 21
Biochemical and Biophysical Research Communications|February 27, 1981
Immunoreactive Cu SOD and Mn SOD in the circulating blood cells from normal and trisomy 21 subjectsA Baret, M A Baeteman, J F Mattei, et al.
Hemoglobin|September 8, 1998
A novel polymorphism 3' to the beta-globin geneC Badens, T Merghoub, D Lena-Russo, et al.
Pediatrie|January 1, 1978
[Neuroleptic poisoning in childhood]G Bosvieux, M C Galland, C Tomasi, et al.
Annales De Genetique|January 1, 1989
[Diagnosis of minor chromosome modifications by molecular cytogenetics]S Taviaux, A Moncla, F Giraud, et al.
Journal De Genetique Humaine|November 1, 1976
[The diminished forms of ectroprosopia: case report with unilateral proboscis]F Giraud, H Bureau, J B Saracco, et al.
Human Genetics|January 1, 1981
Morquio syndrome: clinical findings in 11 patients with MPS IVA and 2 patients with MPS IVBW Holzgreve, H Gröbe, K von Figura, et al.
Journal De Genetique Humaine|December 1, 1981
[Association, in the same subject, of deletion of the short arm of chromosome 4 (4p-) and of complete deficiency of parahydroxyphenyl-pyruvate oxidase activity in the liver (tyrosinosis)]G Malpuech, J F Mattei, J Gaulme, et al.
Marseille Medical|January 1, 1971
[Clinical, mitotic and meiotic study of a trisomy 21 with diabetes in a 52 year old man]F Giraud, J M Luciani, J F Mattei, et al.
Journal of Mental Deficiency Research|September 1, 1979
Erythrocyte copper levels in children with trisomy 21B Mallet, P Poulet, S Ayme, et al.
Human Genetics|January 1, 1987
Monosomy 21: a new case confirmed by in situ hybridizationM C Pellissier, N Philip, M A Voelckel-Baeteman, et al.
Pageof 21