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Annales De Dermatologie Et De Venereologie
|
January 21, 2015
[Recommendations for genetic testing and management of individuals genetically at-risk of cutaneous melanoma]
M-F Avril, P Bahadoran, O Cabaret, et al.
Journal of Neurology
|
August 28, 2010
Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arrays
D H'mida-Ben Brahim, A M'zahem, M Assoum, et al.
Breast Cancer Research and Treatment
|
August 27, 2013
Lack of referral for genetic counseling and testing in BRCA1/2 and Lynch syndromes: a nationwide study based on 240,134 consultations and 134,652 genetic tests
P Pujol, D Stoppa Lyonnet, T Frebourg, et al.
Breast Cancer Research and Treatment
|
April 6, 2012
Rare germline large rearrangements in the BRCA1/2 genes and eight candidate genes in 472 patients with breast cancer predisposition
E Rouleau, B Jesson, A Briaux, et al.
American Journal of Human Genetics
|
February 1, 1996
Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study
S L Neuhausen, S Mazoyer, L Friedman, et al.
Scientific Reports
|
November 12, 2017
Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein
L L Mariani, S Rivaud-Péchoux, P Charles, et al.
Oncogene
|
June 2, 2015
Breast and ovarian cancer predisposition due to de novo BRCA1 and BRCA2 mutations
L Golmard, C Delnatte, A Laugé, et al.
Bulletin Du Cancer
|
July 19, 2001
[Li-Fraumeni syndrome: update, new data and guidelines for clinical management]
T Frebourg, A Abel, C Bonaiti-Pellie, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
March 31, 2000
The pathology of familial breast cancer: histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2
S R Lakhani, B A Gusterson, J Jacquemier, et al.
American Journal of Human Genetics
|
June 19, 1998
Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study
S L Neuhausen, A K Godwin, R Gershoni-Baruch, et al.
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of 10
Search research articles
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Showing results (81-90 of 99) with videos related to
Sort By:
Page
of 10
Annales De Dermatologie Et De Venereologie
|
January 21, 2015
[Recommendations for genetic testing and management of individuals genetically at-risk of cutaneous melanoma]
M-F Avril, P Bahadoran, O Cabaret, et al.
Journal of Neurology
|
August 28, 2010
Molecular diagnosis of known recessive ataxias by homozygosity mapping with SNP arrays
D H'mida-Ben Brahim, A M'zahem, M Assoum, et al.
Breast Cancer Research and Treatment
|
August 27, 2013
Lack of referral for genetic counseling and testing in BRCA1/2 and Lynch syndromes: a nationwide study based on 240,134 consultations and 134,652 genetic tests
P Pujol, D Stoppa Lyonnet, T Frebourg, et al.
Breast Cancer Research and Treatment
|
April 6, 2012
Rare germline large rearrangements in the BRCA1/2 genes and eight candidate genes in 472 patients with breast cancer predisposition
E Rouleau, B Jesson, A Briaux, et al.
American Journal of Human Genetics
|
February 1, 1996
Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study
S L Neuhausen, S Mazoyer, L Friedman, et al.
Scientific Reports
|
November 12, 2017
Comparing ataxias with oculomotor apraxia: a multimodal study of AOA1, AOA2 and AT focusing on video-oculography and alpha-fetoprotein
L L Mariani, S Rivaud-Péchoux, P Charles, et al.
Oncogene
|
June 2, 2015
Breast and ovarian cancer predisposition due to de novo BRCA1 and BRCA2 mutations
L Golmard, C Delnatte, A Laugé, et al.
Bulletin Du Cancer
|
July 19, 2001
[Li-Fraumeni syndrome: update, new data and guidelines for clinical management]
T Frebourg, A Abel, C Bonaiti-Pellie, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research
|
March 31, 2000
The pathology of familial breast cancer: histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2
S R Lakhani, B A Gusterson, J Jacquemier, et al.
American Journal of Human Genetics
|
June 19, 1998
Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study
S L Neuhausen, A K Godwin, R Gershoni-Baruch, et al.
Page
of 10