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 (91-100 of 202) with videos related to

Pageof 21
Sort By:
Human Genetics|January 1, 1988
Assignment of the human progesterone receptor to the q22 band of chromosome 11M G Mattei, A Krust, U Stropp, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Fine mapping of the long arm of human chromosome 11 by in situ hybridization using different translocations, including the t(11;22) of Ewing sarcomaD Bérubé, E Passage, M G Mattei, et al.
Humangenetik|November 6, 1975
[Trisomy 4p. Three new observations (author's transl)]F Giraud, J F Mattei, M G Mattei, et al.
Human Genetics|February 29, 1976
Nonrandom distribution of chromosome breaks in cultured lymphocytes of normal subjectsS Aymé, J F Mattei, M G Mattei, et al.
Annales De Pediatrie|December 1, 1978
[Wilson's disease. Anatomo-clinical study of six cases]P Chapoy, H Perrimond, A M Dor, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|March 8, 1979
[Wilson's disease. A clinical and pathological study on 6 cases (author's transl)]P Chapoy, H Perrimond, A M Dor, et al.
Bulletin Des Societes D'Ophtalmologie De France|May 1, 1975
[Case of unilateral proboscis]J B Saracco, F Giraud, D Fonta, et al.
Human Genetics|January 1, 1981
X-linked mental retardation with the fragile X. A study of 15 familiesJ F Mattei, M G Mattei, C Aumeras, et al.
Archives Francaises De Pediatrie|October 1, 1974
[Holt-Oram syndrome (apropos of a familial case concerning 5 generations)]F Giraud, J B Bertozzi, J F Mattei, et al.
Archives Francaises De Pediatrie|August 1, 1974
[Partial deletion of the short arm of an X chromosome]F Giraud, M Hartung, J F Mattei, et al.
Pageof 21

Showing results (91-100 of 202) with videos related to

Sort By:
Pageof 21
Human Genetics|January 1, 1988
Assignment of the human progesterone receptor to the q22 band of chromosome 11M G Mattei, A Krust, U Stropp, et al.
Cytogenetics and Cell Genetics|January 1, 1990
Fine mapping of the long arm of human chromosome 11 by in situ hybridization using different translocations, including the t(11;22) of Ewing sarcomaD Bérubé, E Passage, M G Mattei, et al.
Humangenetik|November 6, 1975
[Trisomy 4p. Three new observations (author's transl)]F Giraud, J F Mattei, M G Mattei, et al.
Human Genetics|February 29, 1976
Nonrandom distribution of chromosome breaks in cultured lymphocytes of normal subjectsS Aymé, J F Mattei, M G Mattei, et al.
Annales De Pediatrie|December 1, 1978
[Wilson's disease. Anatomo-clinical study of six cases]P Chapoy, H Perrimond, A M Dor, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|March 8, 1979
[Wilson's disease. A clinical and pathological study on 6 cases (author's transl)]P Chapoy, H Perrimond, A M Dor, et al.
Bulletin Des Societes D'Ophtalmologie De France|May 1, 1975
[Case of unilateral proboscis]J B Saracco, F Giraud, D Fonta, et al.
Human Genetics|January 1, 1981
X-linked mental retardation with the fragile X. A study of 15 familiesJ F Mattei, M G Mattei, C Aumeras, et al.
Archives Francaises De Pediatrie|October 1, 1974
[Holt-Oram syndrome (apropos of a familial case concerning 5 generations)]F Giraud, J B Bertozzi, J F Mattei, et al.
Archives Francaises De Pediatrie|August 1, 1974
[Partial deletion of the short arm of an X chromosome]F Giraud, M Hartung, J F Mattei, et al.
Pageof 21