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American Journal of Human Genetics
|
June 1, 1994
Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia I
C Jodice, P Malaspina, F Persichetti, et al.
Brain : a Journal of Neurology
|
December 1, 1992
Autosomal dominant pure cerebellar ataxia. Neurological and genetic study
M Frontali, M Spadaro, P Giunti, et al.
Advances in Neurology
|
January 1, 1993
Linkage studies in dominantly inherited ataxias
H Y Zoghbi, M Frontali, H T Orr, et al.
American Journal of Human Genetics
|
February 1, 1991
Protection against malaria morbidity: near-fixation of the alpha-thalassemia gene in a Nepalese population
G Modiano, G Morpurgo, L Terrenato, et al.
Journal of Molecular Evolution
|
June 1, 1997
Characterization of a small family (CAIII) of microsatellite-containing sequences with X-Y homology
P Malaspina, B M Ciminelli, L Viggiano, et al.
Human Genetics
|
February 1, 1989
Frequency and molecular types of deletional alpha-thalassemia in Egypt
A Novelletto, M Hafez, A Di Rienzo, et al.
Annals of Human Genetics
|
September 1, 1996
Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansions
M Frontali, G Sabbadini, A Novelletto, et al.
American Journal of Human Genetics
|
March 1, 1972
Survey of several red cell and serum genetic markers in a Peruvian population
G Modiano, L Bernini, N D Carter, et al.
Annals of Human Genetics
|
April 22, 2006
Population structure in the Mediterranean basin: a Y chromosome perspective
C Capelli, N Redhead, V Romano, et al.
Molecular Phylogenetics and Evolution
|
August 21, 2003
Clinal patterns of human Y chromosomal diversity in continental Italy and Greece are dominated by drift and founder effects
F Di Giacomo, F Luca, N Anagnou, et al.
Page
of 6
Search research articles
Search
Showing results (41-50 of 56) with videos related to
Sort By:
Page
of 6
American Journal of Human Genetics
|
June 1, 1994
Effect of trinucleotide repeat length and parental sex on phenotypic variation in spinocerebellar ataxia I
C Jodice, P Malaspina, F Persichetti, et al.
Brain : a Journal of Neurology
|
December 1, 1992
Autosomal dominant pure cerebellar ataxia. Neurological and genetic study
M Frontali, M Spadaro, P Giunti, et al.
Advances in Neurology
|
January 1, 1993
Linkage studies in dominantly inherited ataxias
H Y Zoghbi, M Frontali, H T Orr, et al.
American Journal of Human Genetics
|
February 1, 1991
Protection against malaria morbidity: near-fixation of the alpha-thalassemia gene in a Nepalese population
G Modiano, G Morpurgo, L Terrenato, et al.
Journal of Molecular Evolution
|
June 1, 1997
Characterization of a small family (CAIII) of microsatellite-containing sequences with X-Y homology
P Malaspina, B M Ciminelli, L Viggiano, et al.
Human Genetics
|
February 1, 1989
Frequency and molecular types of deletional alpha-thalassemia in Egypt
A Novelletto, M Hafez, A Di Rienzo, et al.
Annals of Human Genetics
|
September 1, 1996
Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: a population genetics model for CAG repeat expansions
M Frontali, G Sabbadini, A Novelletto, et al.
American Journal of Human Genetics
|
March 1, 1972
Survey of several red cell and serum genetic markers in a Peruvian population
G Modiano, L Bernini, N D Carter, et al.
Annals of Human Genetics
|
April 22, 2006
Population structure in the Mediterranean basin: a Y chromosome perspective
C Capelli, N Redhead, V Romano, et al.
Molecular Phylogenetics and Evolution
|
August 21, 2003
Clinal patterns of human Y chromosomal diversity in continental Italy and Greece are dominated by drift and founder effects
F Di Giacomo, F Luca, N Anagnou, et al.
Page
of 6