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La Revue De Medecine Interne
|
February 16, 2005
[HNPCC syndrome (hereditary non polyposis colon cancer): identification and management]
S Olschwang, C Bonaïti, J Feingold, et al.
Journal of Medical Genetics
|
January 31, 2006
Mutations of the RET gene in isolated and syndromic Hirschsprung's disease in human disclose major and modifier alleles at a single locus
L de Pontual, A Pelet, D Trochet, et al.
European Journal of Human Genetics : EJHG
|
September 14, 1999
Genetic polymorphism of the mannose-binding protein gene in children with sickle cell disease: identification of three new variant alleles and relationship to infections
M G Neonato, C Y Lu, M Guilloud-Bataille, et al.
Journal of Medical Genetics
|
March 4, 2005
Homozygosity for a frequent and weakly penetrant predisposing allele at the RET locus in sporadic Hirschsprung disease
A Pelet, L de Pontual, M Clément-Ziza, et al.
Pathologie-Biologie
|
May 9, 2006
[Identification and management of HNPCC syndrome (hereditary non polyposis colon cancer), hereditary predisposition to colorectal and endometrial adenocarcinomas]
S Olschwang, C Bonaïti-Pellié, J Feingold, et al.
Leukemia
|
February 20, 2003
Gemtuzumab ozogamicin in pediatric CD33-positive acute lymphoblastic leukemia: first clinical experiences and relation with cellular sensitivity to single agent calicheamicin
C M Zwaan, D Reinhardt, H Jürgens, et al.
European Journal of Human Genetics : EJHG
|
February 15, 2001
CFTR and asthma in the French EGEA study
R de Cid, J C Chomel, C Lazaro, et al.
Annales De Genetique
|
August 6, 1999
Linkage analysis of 5 novel van der Woude syndrome kindreds to 1q32-q41 markers further supports locus homogeneity of the disease trait
C Houdayer, V Soupre, M Rosenberg-Bourgin, et al.
European Heart Journal
|
March 21, 1998
Genotype-phenotype correlations in familial hypertrophic cardiomyopathy. A comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genes
P Charron, O Dubourg, M Desnos, et al.
Journal of Molecular and Cellular Cardiology
|
February 1, 1997
The influence of the angiotensin I converting enzyme genotype in familial hypertrophic cardiomyopathy varies with the disease gene mutation
F Tesson, C Dufour, J C Moolman, et al.
Page
of 31
Search research articles
Search
Showing results (271-280 of 307) with videos related to
Sort By:
Page
of 31
La Revue De Medecine Interne
|
February 16, 2005
[HNPCC syndrome (hereditary non polyposis colon cancer): identification and management]
S Olschwang, C Bonaïti, J Feingold, et al.
Journal of Medical Genetics
|
January 31, 2006
Mutations of the RET gene in isolated and syndromic Hirschsprung's disease in human disclose major and modifier alleles at a single locus
L de Pontual, A Pelet, D Trochet, et al.
European Journal of Human Genetics : EJHG
|
September 14, 1999
Genetic polymorphism of the mannose-binding protein gene in children with sickle cell disease: identification of three new variant alleles and relationship to infections
M G Neonato, C Y Lu, M Guilloud-Bataille, et al.
Journal of Medical Genetics
|
March 4, 2005
Homozygosity for a frequent and weakly penetrant predisposing allele at the RET locus in sporadic Hirschsprung disease
A Pelet, L de Pontual, M Clément-Ziza, et al.
Pathologie-Biologie
|
May 9, 2006
[Identification and management of HNPCC syndrome (hereditary non polyposis colon cancer), hereditary predisposition to colorectal and endometrial adenocarcinomas]
S Olschwang, C Bonaïti-Pellié, J Feingold, et al.
Leukemia
|
February 20, 2003
Gemtuzumab ozogamicin in pediatric CD33-positive acute lymphoblastic leukemia: first clinical experiences and relation with cellular sensitivity to single agent calicheamicin
C M Zwaan, D Reinhardt, H Jürgens, et al.
European Journal of Human Genetics : EJHG
|
February 15, 2001
CFTR and asthma in the French EGEA study
R de Cid, J C Chomel, C Lazaro, et al.
Annales De Genetique
|
August 6, 1999
Linkage analysis of 5 novel van der Woude syndrome kindreds to 1q32-q41 markers further supports locus homogeneity of the disease trait
C Houdayer, V Soupre, M Rosenberg-Bourgin, et al.
European Heart Journal
|
March 21, 1998
Genotype-phenotype correlations in familial hypertrophic cardiomyopathy. A comparison between mutations in the cardiac protein-C and the beta-myosin heavy chain genes
P Charron, O Dubourg, M Desnos, et al.
Journal of Molecular and Cellular Cardiology
|
February 1, 1997
The influence of the angiotensin I converting enzyme genotype in familial hypertrophic cardiomyopathy varies with the disease gene mutation
F Tesson, C Dufour, J C Moolman, et al.
Page
of 31