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British Journal of Haematology|December 31, 1997

De novo methylation of tumour suppressor genes CDKN2A and CDKN2B is a rare finding in B-cell chronic lymphocytic leukaemiaV Martel, A Guerci, J C Humbert, et al.

Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1997

[Familial supravalvular aortic stenosis. Investigation in a family and review of the literature]P Burnel, F Marçon, H Lucron, et al.

Blood|February 9, 1999

The t(6;8)(q27;p11) translocation in a stem cell myeloproliferative disorder fuses a novel gene, FOP, to fibroblast growth factor receptor 1C Popovici, B Zhang, M J Grégoire, et al.

Human Genetics|December 1, 1993

Chromosomal localization of 9 KOX zinc finger genes: physical linkages suggest clustering of KOX genes on chromosomes 12, 16, and 19M F Rousseau-Merck, J Hillion, P Jonveaux, et al.

Human Mutation|January 1, 1994

Exhaustive analysis of the P53 gene coding sequence by denaturing gradient gel electrophoresis: application to the detection of point mutations in acute leukemiasJ M Pignon, I Vinatier, P Fanen, et al.

Human Reproduction (Oxford, England)|July 20, 2021

Overview of hospitalizations in women undergoing oocyte retrieval for ART in the French national health data systemG Lemardeley, O Pirrello, S Dieterlé, et al.

Nouvelle Revue Francaise D'Hematologie|January 1, 1990

Rearrangement and expression of the p53 gene in myelodysplastic syndrome and acute myeloid leukemiaP Fenaux, M Collyn d'Hooghe, P Jonveaux, et al.

Oncogene|August 1, 1991

Two site-specific deletions and t(1;14) translocation restricted to human T-cell acute leukemias disrupt the 5' part of the tal-1 geneO Bernard, N Lecointe, P Jonveaux, et al.

Leukemia|October 1, 1989

Acute nonlymphocytic leukemia with marrow eosinophilia and chromosome 16 abnormality: a report of 18 casesP Bernard, D Dachary, J Reiffers, et al.

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 30, 2007

[Family study allows more optimistic prognosis and genetic counselling in a child with a deletion of exons 50-51 of the dystrophin gene]G Lesca, H Testard, N Streichenberger, et al.

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Showing results (51-60 of 99) with videos related to

Sort By:

Pageof 10

British Journal of Haematology|December 31, 1997

De novo methylation of tumour suppressor genes CDKN2A and CDKN2B is a rare finding in B-cell chronic lymphocytic leukaemiaV Martel, A Guerci, J C Humbert, et al.

Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1997

[Familial supravalvular aortic stenosis. Investigation in a family and review of the literature]P Burnel, F Marçon, H Lucron, et al.

Blood|February 9, 1999

The t(6;8)(q27;p11) translocation in a stem cell myeloproliferative disorder fuses a novel gene, FOP, to fibroblast growth factor receptor 1C Popovici, B Zhang, M J Grégoire, et al.

Human Genetics|December 1, 1993

Chromosomal localization of 9 KOX zinc finger genes: physical linkages suggest clustering of KOX genes on chromosomes 12, 16, and 19M F Rousseau-Merck, J Hillion, P Jonveaux, et al.

Human Mutation|January 1, 1994

Exhaustive analysis of the P53 gene coding sequence by denaturing gradient gel electrophoresis: application to the detection of point mutations in acute leukemiasJ M Pignon, I Vinatier, P Fanen, et al.

Human Reproduction (Oxford, England)|July 20, 2021

Overview of hospitalizations in women undergoing oocyte retrieval for ART in the French national health data systemG Lemardeley, O Pirrello, S Dieterlé, et al.

Nouvelle Revue Francaise D'Hematologie|January 1, 1990

Rearrangement and expression of the p53 gene in myelodysplastic syndrome and acute myeloid leukemiaP Fenaux, M Collyn d'Hooghe, P Jonveaux, et al.

Oncogene|August 1, 1991

Two site-specific deletions and t(1;14) translocation restricted to human T-cell acute leukemias disrupt the 5' part of the tal-1 geneO Bernard, N Lecointe, P Jonveaux, et al.

Leukemia|October 1, 1989

Acute nonlymphocytic leukemia with marrow eosinophilia and chromosome 16 abnormality: a report of 18 casesP Bernard, D Dachary, J Reiffers, et al.

Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 30, 2007

[Family study allows more optimistic prognosis and genetic counselling in a child with a deletion of exons 50-51 of the dystrophin gene]G Lesca, H Testard, N Streichenberger, et al.

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