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European Journal of Human Genetics : EJHG
|
October 3, 2002
Testing for BRCA1 mutations: a cost-effectiveness analysis
Christine Sevilla, Jean-Paul Moatti, Claire Julian-Reynier, et al.
Human Mutation
|
February 19, 2009
Quantitative PCR high-resolution melting (qPCR-HRM) curve analysis, a new approach to simultaneously screen point mutations and large rearrangements: application to MLH1 germline mutations in Lynch syndrome
Etienne Rouleau, Cédrick Lefol, Violaine Bourdon, et al.
Familial Cancer
|
September 14, 2016
Mutational analysis of TP53 gene in Tunisian familial hematological malignancies and sporadic acute leukemia cases
Walid Sabri Hamadou, Sawsen Besbes, Violaine Bourdon, et al.
Genes, Chromosomes & Cancer
|
January 17, 2002
Genome-wide search for loss of heterozygosity in Burkitt lymphoma cell lines
Hagay Sobol, Athmane Benziane, Fabienne Kerangueven, et al.
Bulletin Du Cancer
|
May 30, 2021
An overview of genetic predisposition to familial hematological malignancies
Walid Sabri Hamadou, Nouha Bouali, Sawsen Besbes, et al.
Bulletin Du Cancer
|
July 10, 2004
[Identification and management of HNPCC syndrome (hereditary non polyposis colon cancer), hereditary predisposition to colorectal and endometrial adenocarcinomas]
Sylviane Olschwang, Catherine Bonaïti, Josué Feingold, et al.
The Prostate
|
February 18, 2021
Bayesian predictive model to assess BRCA2 mutational status according to clinical history: Early onset, metastatic phenotype or family history of breast/ovary cancer
Priscilla Leon, Geraldine Cancel-Tassin, Violaine Bourdon, et al.
Journal of Medical Genetics
|
August 6, 2010
Germline APC mutation spectrum derived from 863 genomic variations identified through a 15-year medical genetics service to French patients with FAP
Arnaud Lagarde, Etienne Rouleau, Anthony Ferrari, et al.
Blood
|
April 10, 2009
High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder
Claude Preudhomme, Aline Renneville, Violaine Bourdon, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
February 1, 2005
Phenotypic heterogeneity in multiple myeloma families
Henry T Lynch, Patrice Watson, Stefano Tarantolo, et al.
Page
of 7
Search research articles
Search
Showing results (11-20 of 65) with videos related to
Sort By:
Page
of 7
European Journal of Human Genetics : EJHG
|
October 3, 2002
Testing for BRCA1 mutations: a cost-effectiveness analysis
Christine Sevilla, Jean-Paul Moatti, Claire Julian-Reynier, et al.
Human Mutation
|
February 19, 2009
Quantitative PCR high-resolution melting (qPCR-HRM) curve analysis, a new approach to simultaneously screen point mutations and large rearrangements: application to MLH1 germline mutations in Lynch syndrome
Etienne Rouleau, Cédrick Lefol, Violaine Bourdon, et al.
Familial Cancer
|
September 14, 2016
Mutational analysis of TP53 gene in Tunisian familial hematological malignancies and sporadic acute leukemia cases
Walid Sabri Hamadou, Sawsen Besbes, Violaine Bourdon, et al.
Genes, Chromosomes & Cancer
|
January 17, 2002
Genome-wide search for loss of heterozygosity in Burkitt lymphoma cell lines
Hagay Sobol, Athmane Benziane, Fabienne Kerangueven, et al.
Bulletin Du Cancer
|
May 30, 2021
An overview of genetic predisposition to familial hematological malignancies
Walid Sabri Hamadou, Nouha Bouali, Sawsen Besbes, et al.
Bulletin Du Cancer
|
July 10, 2004
[Identification and management of HNPCC syndrome (hereditary non polyposis colon cancer), hereditary predisposition to colorectal and endometrial adenocarcinomas]
Sylviane Olschwang, Catherine Bonaïti, Josué Feingold, et al.
The Prostate
|
February 18, 2021
Bayesian predictive model to assess BRCA2 mutational status according to clinical history: Early onset, metastatic phenotype or family history of breast/ovary cancer
Priscilla Leon, Geraldine Cancel-Tassin, Violaine Bourdon, et al.
Journal of Medical Genetics
|
August 6, 2010
Germline APC mutation spectrum derived from 863 genomic variations identified through a 15-year medical genetics service to French patients with FAP
Arnaud Lagarde, Etienne Rouleau, Anthony Ferrari, et al.
Blood
|
April 10, 2009
High frequency of RUNX1 biallelic alteration in acute myeloid leukemia secondary to familial platelet disorder
Claude Preudhomme, Aline Renneville, Violaine Bourdon, et al.
Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology
|
February 1, 2005
Phenotypic heterogeneity in multiple myeloma families
Henry T Lynch, Patrice Watson, Stefano Tarantolo, et al.
Page
of 7