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Human Genetics
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December 29, 2000
Alu insertion polymorphisms in NW Africa and the Iberian Peninsula: evidence for a strong genetic boundary through the Gibraltar Straits
D Comas, F Calafell, N Benchemsi, et al.
Human Heredity
|
January 1, 1997
Haptoglobin phenotypes and gene frequencies in bipolar disorder: an association study in family-history subgroups
L Fãnanás, P Moral, B Gutiérrez, et al.
American Journal of Human Genetics
|
December 6, 2000
Worldwide genetic analysis of the CFTR region
E Mateu, F Calafell, O Lao, et al.
Biological Psychiatry
|
June 5, 1998
Serotonin transporter gene and risk for bipolar affective disorder: an association study in Spanish population
B Gutiérrez, M J Arranz, D A Collier, et al.
Neuroscience Letters
|
January 21, 2004
Variation of the prion gene in chimpanzees and its implication for prion diseases
M Soldevila, A M Andrés, A Blancher, et al.
American Journal of Human Genetics
|
December 1, 1999
Variation in short tandem repeats is deeply structured by genetic background on the human Y chromosome
E Bosch, F Calafell, F R Santos, et al.
Annals of Human Genetics
|
September 6, 2005
The genetics of the pre-Roman Iberian Peninsula: a mtDNA study of ancient Iberians
M L Sampietro, D Caramelli, O Lao, et al.
Nature Genetics
|
June 1, 1994
The origin of the major cystic fibrosis mutation (delta F508) in European populations
N Morral, J Bertranpetit, X Estivill, et al.
International Journal of Legal Medicine
|
February 24, 2001
Y chromosome STR haplotypes in four populations from northwest Africa
E Bosch, F Calafell, A Pérez-Lezaun, et al.
Annals of Human Genetics
|
March 11, 2004
Alu insertion polymorphisms in the Balkans and the origins of the Aromuns
D Comas, H Schmid, S Braeuer, et al.
Page
of 10
Search research articles
Search
Showing results (71-80 of 95) with videos related to
Sort By:
Page
of 10
Human Genetics
|
December 29, 2000
Alu insertion polymorphisms in NW Africa and the Iberian Peninsula: evidence for a strong genetic boundary through the Gibraltar Straits
D Comas, F Calafell, N Benchemsi, et al.
Human Heredity
|
January 1, 1997
Haptoglobin phenotypes and gene frequencies in bipolar disorder: an association study in family-history subgroups
L Fãnanás, P Moral, B Gutiérrez, et al.
American Journal of Human Genetics
|
December 6, 2000
Worldwide genetic analysis of the CFTR region
E Mateu, F Calafell, O Lao, et al.
Biological Psychiatry
|
June 5, 1998
Serotonin transporter gene and risk for bipolar affective disorder: an association study in Spanish population
B Gutiérrez, M J Arranz, D A Collier, et al.
Neuroscience Letters
|
January 21, 2004
Variation of the prion gene in chimpanzees and its implication for prion diseases
M Soldevila, A M Andrés, A Blancher, et al.
American Journal of Human Genetics
|
December 1, 1999
Variation in short tandem repeats is deeply structured by genetic background on the human Y chromosome
E Bosch, F Calafell, F R Santos, et al.
Annals of Human Genetics
|
September 6, 2005
The genetics of the pre-Roman Iberian Peninsula: a mtDNA study of ancient Iberians
M L Sampietro, D Caramelli, O Lao, et al.
Nature Genetics
|
June 1, 1994
The origin of the major cystic fibrosis mutation (delta F508) in European populations
N Morral, J Bertranpetit, X Estivill, et al.
International Journal of Legal Medicine
|
February 24, 2001
Y chromosome STR haplotypes in four populations from northwest Africa
E Bosch, F Calafell, A Pérez-Lezaun, et al.
Annals of Human Genetics
|
March 11, 2004
Alu insertion polymorphisms in the Balkans and the origins of the Aromuns
D Comas, H Schmid, S Braeuer, et al.
Page
of 10