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Human Genetics
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July 1, 1988
cDNA cloning, expression and mapping of human laminin B2 gene to chromosome 1q31
M G Mattei, D Weil, D Pribula-Conway, et al.
Nature
|
March 2, 1995
Defective myosin VIIA gene responsible for Usher syndrome type 1B
D Weil, S Blanchard, J Kaplan, et al.
Annales De Genetique
|
January 1, 1982
[Localization of the gene for ribulose-5-phosphate-3-epimerase on the 2q32 to 2qter segment by interspecies cellular hybridization]
M S Gross, D Weil, Nguyen Van Cong, et al.
American Journal of Human Genetics
|
June 1, 1989
Human nidogen: cDNA cloning, cellular expression, and mapping of the gene to chromosome Iq43
D R Olsen, T Nagayoshi, M Fazio, et al.
Annales De Genetique
|
January 1, 1984
The structural gene for transferrin (TF) maps to 3q21----3qter
C Huerre, G Uzan, K H Grzeschik, et al.
Annals of Human Genetics
|
January 1, 1973
Linkage studies of enzyme markers in man-mouse somatic cell hybrids
C Billardon, Nguyen-Van-Cong, J Y Picard, et al.
The Cancer Journal From Scientific American
|
July 1, 1997
Adult medulloblastoma: an analysis of survival and prognostic factors
Q T Le, M D Weil, W M Wara, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 16, 1996
Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia
D Weil, G Levy, I Sahly, et al.
Human Genetics
|
January 1, 1985
Isolation and characterisation of a cDNA clone for human apolipoprotein CI and assignment of the gene to chromosome 19
F Tata, I Henry, A F Markham, et al.
American Journal of Human Genetics
|
March 1, 1988
Cloning and chromosomal localization of human genes encoding the three chains of type VI collagen
D Weil, M G Mattei, E Passage, et al.
Page
of 21
Search research articles
Search
Showing results (171-180 of 203) with videos related to
Sort By:
Page
of 21
Human Genetics
|
July 1, 1988
cDNA cloning, expression and mapping of human laminin B2 gene to chromosome 1q31
M G Mattei, D Weil, D Pribula-Conway, et al.
Nature
|
March 2, 1995
Defective myosin VIIA gene responsible for Usher syndrome type 1B
D Weil, S Blanchard, J Kaplan, et al.
Annales De Genetique
|
January 1, 1982
[Localization of the gene for ribulose-5-phosphate-3-epimerase on the 2q32 to 2qter segment by interspecies cellular hybridization]
M S Gross, D Weil, Nguyen Van Cong, et al.
American Journal of Human Genetics
|
June 1, 1989
Human nidogen: cDNA cloning, cellular expression, and mapping of the gene to chromosome Iq43
D R Olsen, T Nagayoshi, M Fazio, et al.
Annales De Genetique
|
January 1, 1984
The structural gene for transferrin (TF) maps to 3q21----3qter
C Huerre, G Uzan, K H Grzeschik, et al.
Annals of Human Genetics
|
January 1, 1973
Linkage studies of enzyme markers in man-mouse somatic cell hybrids
C Billardon, Nguyen-Van-Cong, J Y Picard, et al.
The Cancer Journal From Scientific American
|
July 1, 1997
Adult medulloblastoma: an analysis of survival and prognostic factors
Q T Le, M D Weil, W M Wara, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
April 16, 1996
Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia
D Weil, G Levy, I Sahly, et al.
Human Genetics
|
January 1, 1985
Isolation and characterisation of a cDNA clone for human apolipoprotein CI and assignment of the gene to chromosome 19
F Tata, I Henry, A F Markham, et al.
American Journal of Human Genetics
|
March 1, 1988
Cloning and chromosomal localization of human genes encoding the three chains of type VI collagen
D Weil, M G Mattei, E Passage, et al.
Page
of 21