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F Mattei

Showing results (71-80 of 295) with videos related to

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Human Genetics|January 19, 1979
Origin of the extra chromosome in trisomy 21J F Mattei, M G Mattei, S Ayme, et al.
Human Genetics|January 1, 1981
Partial inversion of the secondary constriction of chromosome 9. Does it exist?M G Mattei, J F Mattei, M Guichaoua, et al.
Human Genetics|January 1, 1981
Expression in lymphocyte and fibroblast culture of the fragile X chromosome: a new technical approachM G Mattei, J F Mattei, I Vidal, et al.
Pediatrie|July 1, 1971
[Lyell syndrome and its sequelae in an asthmatic child]E Louchet, L A Gratecos, C Paoli, et al.
Clinical Genetics|September 1, 1983
Familial pericentric inversion of chromosome 9, INV(9)(p22q32) with recurrent duplication-deletionJ F Mattei, M G Mattei, P Balestrazzi, et al.
Journal De Genetique Humaine|March 1, 1982
[Interstitial deletion of chromosome 7 (7q33 to q35)]M Arnolds, M G Mattei, P Rebuffel, et al.
Human Genetics|January 1, 1982
X-autosome translocations: cytogenetic characteristics and their consequencesM G Mattei, J F Mattei, S Ayme, et al.
Human Genetics|September 2, 1979
Partial trisomy 4 resulting from a complex maternal rearrangement of chromosomes 2, 4, and 18 with interstitial translocationM G Mattei, J F Mattei, R Bernard, et al.
Human Genetics|October 28, 1976
Constitutional chromosomal breakageF Giraud, S Ayme, J F Mattei, et al.
Humangenetik|August 25, 1975
[Partial trisomy 11q and familial translocation 11--22 (author's transl)]F Giraud, J F Mattei, M G Mattei, et al.
Pageof 30

Showing results (71-80 of 295) with videos related to

Sort By:
Pageof 30
Human Genetics|January 19, 1979
Origin of the extra chromosome in trisomy 21J F Mattei, M G Mattei, S Ayme, et al.
Human Genetics|January 1, 1981
Partial inversion of the secondary constriction of chromosome 9. Does it exist?M G Mattei, J F Mattei, M Guichaoua, et al.
Human Genetics|January 1, 1981
Expression in lymphocyte and fibroblast culture of the fragile X chromosome: a new technical approachM G Mattei, J F Mattei, I Vidal, et al.
Pediatrie|July 1, 1971
[Lyell syndrome and its sequelae in an asthmatic child]E Louchet, L A Gratecos, C Paoli, et al.
Clinical Genetics|September 1, 1983
Familial pericentric inversion of chromosome 9, INV(9)(p22q32) with recurrent duplication-deletionJ F Mattei, M G Mattei, P Balestrazzi, et al.
Journal De Genetique Humaine|March 1, 1982
[Interstitial deletion of chromosome 7 (7q33 to q35)]M Arnolds, M G Mattei, P Rebuffel, et al.
Human Genetics|January 1, 1982
X-autosome translocations: cytogenetic characteristics and their consequencesM G Mattei, J F Mattei, S Ayme, et al.
Human Genetics|September 2, 1979
Partial trisomy 4 resulting from a complex maternal rearrangement of chromosomes 2, 4, and 18 with interstitial translocationM G Mattei, J F Mattei, R Bernard, et al.
Human Genetics|October 28, 1976
Constitutional chromosomal breakageF Giraud, S Ayme, J F Mattei, et al.
Humangenetik|August 25, 1975
[Partial trisomy 11q and familial translocation 11--22 (author's transl)]F Giraud, J F Mattei, M G Mattei, et al.
Pageof 30