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Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 1, 1991
Tg (9 HSA-MYC), a homozygous lethal insertion in the mouse
S Tutois, J Salaun, M G Mattei, 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.
Biochemistry
|
December 20, 1994
Structure of the mouse dipeptidyl peptidase IV (CD26) gene
A M Bernard, M G Mattei, M Pierres, et al.
Human Genetics
|
March 1, 1990
Assignment by in situ hybridization of the angiotensinogen gene to chromosome band 1q4, the same region as the human renin gene
I Gaillard-Sanchez, M G Mattei, E Clauser, et al.
Human Genetics
|
January 1, 1982
X-autosome translocations: cytogenetic characteristics and their consequences
M G Mattei, J F Mattei, S Ayme, et al.
Cytogenetics and Cell Genetics
|
September 8, 1998
Identification and in situ hybridization mapping of a mouse Tpd52l1 (D53) orthologue to chromosome 10A4-B2
J A Byrne, M G Mattei, P Basset, et al.
Human Genetics
|
September 2, 1979
Partial trisomy 4 resulting from a complex maternal rearrangement of chromosomes 2, 4, and 18 with interstitial translocation
M G Mattei, J F Mattei, R Bernard, et al.
Human Genetics
|
October 28, 1976
Constitutional chromosomal breakage
F 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.
Journal De Genetique Humaine
|
July 1, 1984
[Mental retardation linked to fragility of chromosome X: current knowledge]
J F Mattei, M G Mattei, M Auger, et al.
Page
of 39
Search research articles
Search
Showing results (61-70 of 385) with videos related to
Sort By:
Page
of 39
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
January 1, 1991
Tg (9 HSA-MYC), a homozygous lethal insertion in the mouse
S Tutois, J Salaun, M G Mattei, 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.
Biochemistry
|
December 20, 1994
Structure of the mouse dipeptidyl peptidase IV (CD26) gene
A M Bernard, M G Mattei, M Pierres, et al.
Human Genetics
|
March 1, 1990
Assignment by in situ hybridization of the angiotensinogen gene to chromosome band 1q4, the same region as the human renin gene
I Gaillard-Sanchez, M G Mattei, E Clauser, et al.
Human Genetics
|
January 1, 1982
X-autosome translocations: cytogenetic characteristics and their consequences
M G Mattei, J F Mattei, S Ayme, et al.
Cytogenetics and Cell Genetics
|
September 8, 1998
Identification and in situ hybridization mapping of a mouse Tpd52l1 (D53) orthologue to chromosome 10A4-B2
J A Byrne, M G Mattei, P Basset, et al.
Human Genetics
|
September 2, 1979
Partial trisomy 4 resulting from a complex maternal rearrangement of chromosomes 2, 4, and 18 with interstitial translocation
M G Mattei, J F Mattei, R Bernard, et al.
Human Genetics
|
October 28, 1976
Constitutional chromosomal breakage
F 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.
Journal De Genetique Humaine
|
July 1, 1984
[Mental retardation linked to fragility of chromosome X: current knowledge]
J F Mattei, M G Mattei, M Auger, et al.
Page
of 39