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Genomics
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May 1, 1994
Molecular cloning, cDNA analysis, and localization of a monomer of the N-acetylglucosamine-specific receptor of the thyroid, NAGR1, to chromosome 19p13.3-13.2
O Blanck, C Perrin, H Mziaut, et al.
Nature
|
December 15, 1983
Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male
G Camerino, M G Mattei, J F Mattei, et al.
Human Genetics
|
January 1, 1980
Clinical, enzyme, and cytogenetic investigations in three new cases of trisomy 8p
J F Mattei, M G Mattei, J P Ardissone, et al.
Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]
|
April 1, 1977
Subacute myelocytic leukemia associated with the philadelphia chromosome and supplementary translocation : 9-12
J F Dor, J F Mattei, M G Mattei, et al.
Genetical Research
|
June 1, 1989
Chromosomal localization of the mouse gene coding for vimentin
M G Mattei, A Lilienbaum, L Z Lin, et al.
The Biochemical Journal
|
May 15, 1995
Structural organization and chromosomal localization of the mouse collagenase type I gene
M Schorpp, M G Mattei, I Herr, et al.
Human Genetics
|
July 1, 1994
Chromosomal mapping of human adenylyl cyclase genes type III, type V and type VI
N Haber, D Stengel, N Defer, et al.
Archives Francaises De Pediatrie
|
February 1, 1975
[Trisomy 8 in mosaicism]
F Giraud, J F Mattei, M Blanc-Pardigon, et al.
Immunity
|
January 16, 1998
Genetic control of diabetes progression
A Gonzalez, J D Katz, M G Mattei, et al.
Genomics
|
September 1, 1991
Chromosomal assignments of the genes for neuroendocrine convertase PC1 (NEC1) to human 5q15-21, neuroendocrine convertase PC2 (NEC2) to human 20p11.1-11.2, and furin (mouse 7[D1-E2] region)
N G Seidah, M G Mattei, L Gaspar, et al.
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of 39
Search research articles
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Showing results (151-160 of 385) with videos related to
Sort By:
Page
of 39
Genomics
|
May 1, 1994
Molecular cloning, cDNA analysis, and localization of a monomer of the N-acetylglucosamine-specific receptor of the thyroid, NAGR1, to chromosome 19p13.3-13.2
O Blanck, C Perrin, H Mziaut, et al.
Nature
|
December 15, 1983
Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male
G Camerino, M G Mattei, J F Mattei, et al.
Human Genetics
|
January 1, 1980
Clinical, enzyme, and cytogenetic investigations in three new cases of trisomy 8p
J F Mattei, M G Mattei, J P Ardissone, et al.
Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]
|
April 1, 1977
Subacute myelocytic leukemia associated with the philadelphia chromosome and supplementary translocation : 9-12
J F Dor, J F Mattei, M G Mattei, et al.
Genetical Research
|
June 1, 1989
Chromosomal localization of the mouse gene coding for vimentin
M G Mattei, A Lilienbaum, L Z Lin, et al.
The Biochemical Journal
|
May 15, 1995
Structural organization and chromosomal localization of the mouse collagenase type I gene
M Schorpp, M G Mattei, I Herr, et al.
Human Genetics
|
July 1, 1994
Chromosomal mapping of human adenylyl cyclase genes type III, type V and type VI
N Haber, D Stengel, N Defer, et al.
Archives Francaises De Pediatrie
|
February 1, 1975
[Trisomy 8 in mosaicism]
F Giraud, J F Mattei, M Blanc-Pardigon, et al.
Immunity
|
January 16, 1998
Genetic control of diabetes progression
A Gonzalez, J D Katz, M G Mattei, et al.
Genomics
|
September 1, 1991
Chromosomal assignments of the genes for neuroendocrine convertase PC1 (NEC1) to human 5q15-21, neuroendocrine convertase PC2 (NEC2) to human 20p11.1-11.2, and furin (mouse 7[D1-E2] region)
N G Seidah, M G Mattei, L Gaspar, et al.
Page
of 39