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F Mattei

Showing results (41-50 of 295) with videos related to

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Archives Francaises De Pediatrie|August 1, 1985
[Contribution of in situ hybridization to chromosomal analysis]M G Mattei, J F Mattei, F Giraud
La Presse Medicale|May 9, 1970
[Kwashiorkor at the Dakar University Hospital]P Satge, J F Mattei, M P Gastou
Journal of Immunology (Baltimore, Md. : 1950)|July 24, 2001
IL-15 is expressed by dendritic cells in response to type I IFN, double-stranded RNA, or lipopolysaccharide and promotes dendritic cell activationF Mattei, G Schiavoni, F Belardelli, et al.
American Journal of Medical Genetics|October 1, 1990
Parental origin of del(15)(q11-q13) in Angelman and Prader-Willi syndromesR Zori, C Williams, J F Mattei, et al.
Clinical Genetics|January 1, 1983
X-linked mental retardation, growth retardation, deafness and microgenitalism. A second familial reportJ F Mattei, P Collignon, S Ayme, et al.
American Journal of Medical Genetics|January 1, 1981
Coffin-Lowry syndrome in sibsJ F Mattei, R Laframboise, F Rouault, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1981
[45X/46XY/46XrY mosaic with banding and the Turner phenotype (author's transl)]L Aubert, C Verdet, F Giraud, et al.
Pediatrie|January 1, 1992
[Fragile X syndrome: current knowledge]M C Pellissier, M A Voelckel, J F Mattei
Archives Francaises De Pediatrie|January 1, 1976
[Humoral immunity and blastic transformation of lymphocytes in trisomy 21]R Bernard, S Sitrk, D Bernard, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|April 18, 1979
[Asymetrical gonadal dysgenesis. Report of a case (author's transl)]P Chapoy, J F Mattei, C Exbrayat, et al.
Pageof 30

Showing results (41-50 of 295) with videos related to

Sort By:
Pageof 30
Archives Francaises De Pediatrie|August 1, 1985
[Contribution of in situ hybridization to chromosomal analysis]M G Mattei, J F Mattei, F Giraud
La Presse Medicale|May 9, 1970
[Kwashiorkor at the Dakar University Hospital]P Satge, J F Mattei, M P Gastou
Journal of Immunology (Baltimore, Md. : 1950)|July 24, 2001
IL-15 is expressed by dendritic cells in response to type I IFN, double-stranded RNA, or lipopolysaccharide and promotes dendritic cell activationF Mattei, G Schiavoni, F Belardelli, et al.
American Journal of Medical Genetics|October 1, 1990
Parental origin of del(15)(q11-q13) in Angelman and Prader-Willi syndromesR Zori, C Williams, J F Mattei, et al.
Clinical Genetics|January 1, 1983
X-linked mental retardation, growth retardation, deafness and microgenitalism. A second familial reportJ F Mattei, P Collignon, S Ayme, et al.
American Journal of Medical Genetics|January 1, 1981
Coffin-Lowry syndrome in sibsJ F Mattei, R Laframboise, F Rouault, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1981
[45X/46XY/46XrY mosaic with banding and the Turner phenotype (author's transl)]L Aubert, C Verdet, F Giraud, et al.
Pediatrie|January 1, 1992
[Fragile X syndrome: current knowledge]M C Pellissier, M A Voelckel, J F Mattei
Archives Francaises De Pediatrie|January 1, 1976
[Humoral immunity and blastic transformation of lymphocytes in trisomy 21]R Bernard, S Sitrk, D Bernard, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|April 18, 1979
[Asymetrical gonadal dysgenesis. Report of a case (author's transl)]P Chapoy, J F Mattei, C Exbrayat, et al.
Pageof 30