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American Journal of Medical Genetics
|
July 15, 1994
Haplotype analysis at the FRAXA locus in the Japanese population
R I Richards, I Kondo, K Holman, et al.
Journal of Medical Genetics
|
December 1, 1991
Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site
R I Richards, K Holman, H Kozman, et al.
Nature Genetics
|
July 1, 1992
Evidence of founder chromosomes in fragile X syndrome
R I Richards, K Holman, K Friend, et al.
Nature
|
August 31, 1995
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene
E I Rogaev, R Sherrington, E A Rogaeva, et al.
Science (New York, N.Y.)
|
May 24, 1991
Fragile X genotype characterized by an unstable region of DNA
S Yu, M Pritchard, E Kremer, et al.
American Journal of Human Genetics
|
August 1, 1993
Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studies
I Aksentijevich, E Pras, L Gruberg, et al.
American Journal of Human Genetics
|
September 1, 1993
Familial Mediterranean fever (FMF) in Moroccan Jews: demonstration of a founder effect by extended haplotype analysis
I Aksentijevich, E Pras, L Gruberg, et al.
Genomics
|
July 1, 1994
A PCR-based genetic linkage map of human chromosome 16
Y Shen, H M Kozman, A Thompson, et al.
Science (New York, N.Y.)
|
June 24, 1994
Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis
J K Nancarrow, E Kremer, K Holman, et al.
Science (New York, N.Y.)
|
June 21, 1991
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n
E J Kremer, M Pritchard, M Lynch, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 45) with videos related to
Sort By:
Page
of 5
American Journal of Medical Genetics
|
July 15, 1994
Haplotype analysis at the FRAXA locus in the Japanese population
R I Richards, I Kondo, K Holman, et al.
Journal of Medical Genetics
|
December 1, 1991
Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site
R I Richards, K Holman, H Kozman, et al.
Nature Genetics
|
July 1, 1992
Evidence of founder chromosomes in fragile X syndrome
R I Richards, K Holman, K Friend, et al.
Nature
|
August 31, 1995
Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene
E I Rogaev, R Sherrington, E A Rogaeva, et al.
Science (New York, N.Y.)
|
May 24, 1991
Fragile X genotype characterized by an unstable region of DNA
S Yu, M Pritchard, E Kremer, et al.
American Journal of Human Genetics
|
August 1, 1993
Refined mapping of the gene causing familial Mediterranean fever, by linkage and homozygosity studies
I Aksentijevich, E Pras, L Gruberg, et al.
American Journal of Human Genetics
|
September 1, 1993
Familial Mediterranean fever (FMF) in Moroccan Jews: demonstration of a founder effect by extended haplotype analysis
I Aksentijevich, E Pras, L Gruberg, et al.
Genomics
|
July 1, 1994
A PCR-based genetic linkage map of human chromosome 16
Y Shen, H M Kozman, A Thompson, et al.
Science (New York, N.Y.)
|
June 24, 1994
Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis
J K Nancarrow, E Kremer, K Holman, et al.
Science (New York, N.Y.)
|
June 21, 1991
Mapping of DNA instability at the fragile X to a trinucleotide repeat sequence p(CCG)n
E J Kremer, M Pritchard, M Lynch, et al.
Page
of 5