Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

J-F Mattei

Showing results (31-40 of 202) with videos related to

Pageof 21
Sort By:
European Journal of Human Genetics : EJHG|January 1, 1997
Genetic services in FranceS Aymé, M L Briard, 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
La Presse Medicale|May 9, 1970
[Kwashiorkor at the Dakar University Hospital]P Satge, J F Mattei, M P Gastou
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.
Pageof 21

Showing results (31-40 of 202) with videos related to

Sort By:
Pageof 21
European Journal of Human Genetics : EJHG|January 1, 1997
Genetic services in FranceS Aymé, M L Briard, 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
La Presse Medicale|May 9, 1970
[Kwashiorkor at the Dakar University Hospital]P Satge, J F Mattei, M P Gastou
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.
Pageof 21