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Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
December 1, 1994
cDNA sequence of Aldgh, the mouse homolog of the X-linked adrenoleukodystrophy gene
C O Sarde, J Thomas, H Sadoulet, et al.
FEBS Letters
|
April 1, 1997
Fenofibrate differently alters expression of genes encoding ATP-binding transporter proteins of the peroxisomal membrane
S Albet, C Causeret, M Bentejac, et al.
Cell
|
February 1, 1981
The ovalbumin gene family: hormonal control of X and Y gene transcription and mRNA accumulation
M LeMeur, N Glanville, J L Mandel, 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.
American Journal of Medical Genetics
|
July 15, 1994
Non-specific X-linked mental retardation: linkage analysis in MRX2 and MRX4 families revisited
L J Hu, S Blumenfeld-Heyberger, A Hanauer, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1993
Striking founder effect for the fragile X syndrome in Finland
C Oudet, H von Koskull, A M Nordström, et al.
EXS
|
January 1, 1993
Microsatellites and disease: a new paradigm
K Wrogemann, V Biancalana, D Devys, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1993
Gene in the region of the Friedreich ataxia locus encodes a putative transmembrane protein expressed in the nervous system
F Duclos, U Boschert, G Sirugo, et al.
Human Molecular Genetics
|
July 1, 1992
Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy
V Biancalana, F Serville, J Pommier, et al.
Nucleic Acids Research
|
June 11, 1983
Isolation and characterization of cDNA clones for human skeletal muscle alpha actin
A Hanauer, M Levin, R Heilig, et al.
Page
of 26
Search research articles
Search
Showing results (111-120 of 257) with videos related to
Sort By:
Page
of 26
Mammalian Genome : Official Journal of the International Mammalian Genome Society
|
December 1, 1994
cDNA sequence of Aldgh, the mouse homolog of the X-linked adrenoleukodystrophy gene
C O Sarde, J Thomas, H Sadoulet, et al.
FEBS Letters
|
April 1, 1997
Fenofibrate differently alters expression of genes encoding ATP-binding transporter proteins of the peroxisomal membrane
S Albet, C Causeret, M Bentejac, et al.
Cell
|
February 1, 1981
The ovalbumin gene family: hormonal control of X and Y gene transcription and mRNA accumulation
M LeMeur, N Glanville, J L Mandel, 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.
American Journal of Medical Genetics
|
July 15, 1994
Non-specific X-linked mental retardation: linkage analysis in MRX2 and MRX4 families revisited
L J Hu, S Blumenfeld-Heyberger, A Hanauer, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1993
Striking founder effect for the fragile X syndrome in Finland
C Oudet, H von Koskull, A M Nordström, et al.
EXS
|
January 1, 1993
Microsatellites and disease: a new paradigm
K Wrogemann, V Biancalana, D Devys, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1993
Gene in the region of the Friedreich ataxia locus encodes a putative transmembrane protein expressed in the nervous system
F Duclos, U Boschert, G Sirugo, et al.
Human Molecular Genetics
|
July 1, 1992
Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy
V Biancalana, F Serville, J Pommier, et al.
Nucleic Acids Research
|
June 11, 1983
Isolation and characterization of cDNA clones for human skeletal muscle alpha actin
A Hanauer, M Levin, R Heilig, et al.
Page
of 26