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International Journal of Leprosy and Other Mycobacterial Diseases : Official Organ of the International Leprosy Association
|
June 1, 1989
Genetic susceptibility to leprosy on a Caribbean Island: linkage analysis with five markers
L Abel, F Demenais, M S Baule, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
April 2, 1998
Lack of correlation between genotype and phenotype in celiac disease
L Greco, S Percopo, F Clot, et al.
Psychiatry Research
|
December 1, 1992
Failure to replicate linkage between chromosome 5q11-q13 markers and schizophrenia in 28 families
D Campion, T d'Amato, H Laklou, et al.
Nature Genetics
|
November 1, 1994
A second locus for Marfan syndrome maps to chromosome 3p24.2-p25
G Collod, M C Babron, G Jondeau, et al.
American Journal of Medical Genetics
|
September 15, 1994
Association of apolipoprotein E allele epsilon 4 with late-onset sporadic Alzheimer's disease
G Lucotte, S Visvikis, B Leininger-Müler, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
April 25, 2000
Study of two ectopeptidases in the susceptibility to celiac disease: two newly identified polymorphisms of dipeptidylpeptidase IV
F Clot, M C Babron, S Percopo, et al.
American Journal of Medical Genetics
|
June 19, 1995
Characteristics of familial aggregation in early-onset Alzheimer's disease: evidence of subgroups
D Campion, M Martinez, D Hannequin, et al.
American Journal of Human Genetics
|
July 1, 1993
Autosomal dominant Marfan-like connective-tissue disorder with aortic dilation and skeletal anomalies not linked to the fibrillin genes
C Boileau, G Jondeau, M C Babron, et al.
Pediatrics
|
December 1, 1993
Childhood-onset systemic lupus erythematosus: antiphospholipid antibodies in 37 patients and their first-degree relatives
C Molta, O Meyer, C Dosquet, et al.
American Journal of Medical Genetics
|
February 16, 1996
Segregation analysis of Alzheimer pedigrees: rare Mendelian dominant mutation(s) explain a minority of early-onset cases. French Alzheimer Collaborative Group
M Martinez, D Campion, M C Babron, et al.
Page
of 7
Search research articles
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Showing results (41-50 of 68) with videos related to
Sort By:
Page
of 7
International Journal of Leprosy and Other Mycobacterial Diseases : Official Organ of the International Leprosy Association
|
June 1, 1989
Genetic susceptibility to leprosy on a Caribbean Island: linkage analysis with five markers
L Abel, F Demenais, M S Baule, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
April 2, 1998
Lack of correlation between genotype and phenotype in celiac disease
L Greco, S Percopo, F Clot, et al.
Psychiatry Research
|
December 1, 1992
Failure to replicate linkage between chromosome 5q11-q13 markers and schizophrenia in 28 families
D Campion, T d'Amato, H Laklou, et al.
Nature Genetics
|
November 1, 1994
A second locus for Marfan syndrome maps to chromosome 3p24.2-p25
G Collod, M C Babron, G Jondeau, et al.
American Journal of Medical Genetics
|
September 15, 1994
Association of apolipoprotein E allele epsilon 4 with late-onset sporadic Alzheimer's disease
G Lucotte, S Visvikis, B Leininger-Müler, et al.
Journal of Pediatric Gastroenterology and Nutrition
|
April 25, 2000
Study of two ectopeptidases in the susceptibility to celiac disease: two newly identified polymorphisms of dipeptidylpeptidase IV
F Clot, M C Babron, S Percopo, et al.
American Journal of Medical Genetics
|
June 19, 1995
Characteristics of familial aggregation in early-onset Alzheimer's disease: evidence of subgroups
D Campion, M Martinez, D Hannequin, et al.
American Journal of Human Genetics
|
July 1, 1993
Autosomal dominant Marfan-like connective-tissue disorder with aortic dilation and skeletal anomalies not linked to the fibrillin genes
C Boileau, G Jondeau, M C Babron, et al.
Pediatrics
|
December 1, 1993
Childhood-onset systemic lupus erythematosus: antiphospholipid antibodies in 37 patients and their first-degree relatives
C Molta, O Meyer, C Dosquet, et al.
American Journal of Medical Genetics
|
February 16, 1996
Segregation analysis of Alzheimer pedigrees: rare Mendelian dominant mutation(s) explain a minority of early-onset cases. French Alzheimer Collaborative Group
M Martinez, D Campion, M C Babron, et al.
Page
of 7