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Human Genetics
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December 22, 1998
FRAXE: the HindIII/OXE20 restriction polymorphism is not a rare variant
M Blayau, S Odent, C Dubourg, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 21, 1998
Blood-borne seeding by hematopoietic and endothelial precursors from the allantois
A Caprioli, T Jaffredo, R Gautier, et al.
Bulletin De La Societe De Pathologie Exotique Et De Ses Filiales
|
January 1, 1986
[Malaria in Gabon. I. Study of 500 children with fever in Libreville]
D Richard-Lenoble, M Kombila, J Chandenier, et al.
Human Mutation
|
March 27, 1999
Identification of three novel mutations in the dystrophin gene detected by the heteroduplex/SSCA screening procedure. Mutations in brief no. 222. Online
C Dubourg, S Odent, P Fergelot, et al.
Atherosclerosis
|
February 1, 1994
Identification of the homozygous missense mutation in the lecithin:cholesterol-acyltransferase (LCAT) gene, causing LCAT familial deficiency in two French patients
I Dorval, P Jezequel, C Dubourg, et al.
European Journal of Human Genetics : EJHG
|
October 20, 2000
A new mutation in the six-domain of SIX3 gene causes holoprosencephaly
L Pasquier, C Dubourg, M Blayau, et al.
Journal of Medical Genetics
|
January 7, 2005
First occurrence of aprosencephaly/atelencephaly and holoprosencephaly in a family with a SIX3 gene mutation and phenotype/genotype correlation in our series of SIX3 mutations
L Pasquier, C Dubourg, M Gonzales, et al.
Annales De Biologie Clinique
|
January 9, 2004
[Genetic study of holoprosencephaly]
C Dubourg, L Lazaro, M Blayau, et al.
Cytogenetics and Cell Genetics
|
April 25, 2000
Eukaryotic translation termination factor gene (ETF1/eRF1) maps at D5S500 in a commonly deleted region of chromosome 5q31 in malignant myeloid diseases
L Guenet, C Henry, B Toutain, et al.
Clinical Chemistry
|
December 1, 1994
Rapid detection of 1078 delT mutation by PCR-mediated site-directed mutagenesis: detection of cystic fibrosis carriers in a celtic population
I Dorval, P Fergelot, C Dubourg, et al.
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Search research articles
Search
Showing results (1-10 of 28) with videos related to
Sort By:
Page
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Human Genetics
|
December 22, 1998
FRAXE: the HindIII/OXE20 restriction polymorphism is not a rare variant
M Blayau, S Odent, C Dubourg, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
March 21, 1998
Blood-borne seeding by hematopoietic and endothelial precursors from the allantois
A Caprioli, T Jaffredo, R Gautier, et al.
Bulletin De La Societe De Pathologie Exotique Et De Ses Filiales
|
January 1, 1986
[Malaria in Gabon. I. Study of 500 children with fever in Libreville]
D Richard-Lenoble, M Kombila, J Chandenier, et al.
Human Mutation
|
March 27, 1999
Identification of three novel mutations in the dystrophin gene detected by the heteroduplex/SSCA screening procedure. Mutations in brief no. 222. Online
C Dubourg, S Odent, P Fergelot, et al.
Atherosclerosis
|
February 1, 1994
Identification of the homozygous missense mutation in the lecithin:cholesterol-acyltransferase (LCAT) gene, causing LCAT familial deficiency in two French patients
I Dorval, P Jezequel, C Dubourg, et al.
European Journal of Human Genetics : EJHG
|
October 20, 2000
A new mutation in the six-domain of SIX3 gene causes holoprosencephaly
L Pasquier, C Dubourg, M Blayau, et al.
Journal of Medical Genetics
|
January 7, 2005
First occurrence of aprosencephaly/atelencephaly and holoprosencephaly in a family with a SIX3 gene mutation and phenotype/genotype correlation in our series of SIX3 mutations
L Pasquier, C Dubourg, M Gonzales, et al.
Annales De Biologie Clinique
|
January 9, 2004
[Genetic study of holoprosencephaly]
C Dubourg, L Lazaro, M Blayau, et al.
Cytogenetics and Cell Genetics
|
April 25, 2000
Eukaryotic translation termination factor gene (ETF1/eRF1) maps at D5S500 in a commonly deleted region of chromosome 5q31 in malignant myeloid diseases
L Guenet, C Henry, B Toutain, et al.
Clinical Chemistry
|
December 1, 1994
Rapid detection of 1078 delT mutation by PCR-mediated site-directed mutagenesis: detection of cystic fibrosis carriers in a celtic population
I Dorval, P Fergelot, C Dubourg, et al.
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of 3