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The Journal of Clinical Investigation
|
May 1, 1984
Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX gene
L Grunebaum, J P Cazenave, G Camerino, et al.
Neurology
|
November 1, 1993
Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families
M Ben Hamida, S Belal, G Sirugo, et al.
American Journal of Medical Genetics
|
February 1, 1991
New polymorphism and a new chromosome breakpoint establish the physical and genetic mapping of DXS369 in the DXS98-FRAXA interval
I Oberlé, A Vincent, N Abbadi, et al.
Nature
|
May 10, 1979
The ovalbumin gene region: common features in the organisation of three genes expressed in chicken oviduct under hormonal control
A Royal, A Garapin, B Cami, et al.
Journal of Medical Genetics
|
November 5, 2002
Linkage to 18qter differentiates two clinically overlapping syndromes: congenital cataracts-facial dysmorphism-neuropathy (CCFDN) syndrome and Marinesco-Sjögren syndrome
C Lagier-Tourenne, D Chaigne, J Gong, et al.
Molecular Psychiatry
|
March 24, 1999
Polyglutamine-containing proteins in schizophrenia
R Joober, C Benkelfat, M Jannatipour, et al.
American Journal of Human Genetics
|
October 1, 1996
Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis: analysis of four FRAXE families with mild mental retardation in males
V Biancalana, L Taine, J C Bouix, et al.
Human Genetics
|
December 1, 1989
Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemia
S Guioli, B Arveiler, B Bardoni, et al.
American Journal of Human Genetics
|
March 1, 1985
Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus
B de Martinville, L M Kunkel, G Bruns, et al.
American Journal of Medical Genetics
|
July 15, 1994
Sixth international workshop on the fragile X and X-linked mental retardation
G R Sutherland, W T Brown, R Hagerman, et al.
Page
of 26
Search research articles
Search
Showing results (221-230 of 257) with videos related to
Sort By:
Page
of 26
The Journal of Clinical Investigation
|
May 1, 1984
Carrier detection of Hemophilia B by using a restriction site polymorphism associated with the coagulation Factor IX gene
L Grunebaum, J P Cazenave, G Camerino, et al.
Neurology
|
November 1, 1993
Friedreich's ataxia phenotype not linked to chromosome 9 and associated with selective autosomal recessive vitamin E deficiency in two inbred Tunisian families
M Ben Hamida, S Belal, G Sirugo, et al.
American Journal of Medical Genetics
|
February 1, 1991
New polymorphism and a new chromosome breakpoint establish the physical and genetic mapping of DXS369 in the DXS98-FRAXA interval
I Oberlé, A Vincent, N Abbadi, et al.
Nature
|
May 10, 1979
The ovalbumin gene region: common features in the organisation of three genes expressed in chicken oviduct under hormonal control
A Royal, A Garapin, B Cami, et al.
Journal of Medical Genetics
|
November 5, 2002
Linkage to 18qter differentiates two clinically overlapping syndromes: congenital cataracts-facial dysmorphism-neuropathy (CCFDN) syndrome and Marinesco-Sjögren syndrome
C Lagier-Tourenne, D Chaigne, J Gong, et al.
Molecular Psychiatry
|
March 24, 1999
Polyglutamine-containing proteins in schizophrenia
R Joober, C Benkelfat, M Jannatipour, et al.
American Journal of Human Genetics
|
October 1, 1996
Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis: analysis of four FRAXE families with mild mental retardation in males
V Biancalana, L Taine, J C Bouix, et al.
Human Genetics
|
December 1, 1989
Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemia
S Guioli, B Arveiler, B Bardoni, et al.
American Journal of Human Genetics
|
March 1, 1985
Localization of DNA sequences in region Xp21 of the human X chromosome: search for molecular markers close to the Duchenne muscular dystrophy locus
B de Martinville, L M Kunkel, G Bruns, et al.
American Journal of Medical Genetics
|
July 15, 1994
Sixth international workshop on the fragile X and X-linked mental retardation
G R Sutherland, W T Brown, R Hagerman, et al.
Page
of 26