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F Mattei

Showing results (161-170 of 295) with videos related to

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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.
Annales De Chirurgie|December 1, 1975
[Traumatic rupture of the aortic isthmus. Emergency repair by direct suturing under partly E.C.C. (author's transl)]I Gandjbakhch, L Loygue, M T Cousin, 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.
Presse Medicale (Paris, France : 1983)|December 2, 1992
[Viral pneumopathies after heart transplantation. Radioclinical analysis]F Chabot, L Hennequin, L Moreau, 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.
Human Genetics|December 1, 1988
Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardationM A Voelckel, M G Mattei, C N'Guyen, et al.
Annales De Medecine Interne|May 1, 1978
[Surgical treatment and immediate postoperative results in acute aortic bacterial endocarditis]P Charlier, G Trouillet, M F Mattei, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|February 1, 1976
[Prosthetic valve replacement in children]C Cabrol, A Cabrol, I Gandjbakhch, et al.
Pageof 30

Showing results (161-170 of 295) with videos related to

Sort By:
Pageof 30
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.
Annales De Chirurgie|December 1, 1975
[Traumatic rupture of the aortic isthmus. Emergency repair by direct suturing under partly E.C.C. (author's transl)]I Gandjbakhch, L Loygue, M T Cousin, 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.
Presse Medicale (Paris, France : 1983)|December 2, 1992
[Viral pneumopathies after heart transplantation. Radioclinical analysis]F Chabot, L Hennequin, L Moreau, 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.
Human Genetics|December 1, 1988
Dissociation between mental retardation and fragile site expression in a family with fragile X-linked mental retardationM A Voelckel, M G Mattei, C N'Guyen, et al.
Annales De Medecine Interne|May 1, 1978
[Surgical treatment and immediate postoperative results in acute aortic bacterial endocarditis]P Charlier, G Trouillet, M F Mattei, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|February 1, 1976
[Prosthetic valve replacement in children]C Cabrol, A Cabrol, I Gandjbakhch, et al.
Pageof 30