M Jeanpierre|C Junien - JoVE Visualize

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Human Genetics|June 1, 1997

alpha-satellite DNA methylation in normal individuals and in ICF patients: heterogeneous methylation of constitutive heterochromatin in adult and fetal tissuesP Miniou, M Jeanpierre, D Bourc'his, et al.

Human Genetics|March 1, 1989

Detection of 1q polysomy in interphase nuclei of human solid tumors with a biotinylated probeE Viegas-Péquignot, M Jeanpierre, A M Dutrillaux, et al.

Annales De Genetique|January 1, 1980

[Increase of LDH A and partial trisomy 11p (author's transl)]M O Rethoré, C Junien, A Aurias, et al.

DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|January 1, 1999

cDNA cloning, tissue distribution and chromosomal localization of the human ID4 geneM Rigolet, T Rich, M S Gross-Morand, et al.

Human Molecular Genetics|August 1, 1993

Myotonic dystrophy: absence of CTG enlarged transcript in congenital forms, and low expression of the normal alleleH Hofmann-Radvanyi, C Lavedan, J P Rabès, et al.

Human Genetics|January 1, 1984

Del11p13/nephroblastoma without aniridiaC Turleau, J de Grouchy, C Nihoul-Fékété, et al.

Human Genetics|January 19, 1978

Heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Algeria. Study in Northern Algeria with description of five new variantsM Benabadji, F Merad, M Benmoussa, et al.

Annales De Medecine Interne|November 1, 1977

[Generalized saturnine paralysis. Discovery of a double congenital disease: glucose-6-phosphate dehydrogenase deficiency (new variant) and distal tubular acidosis]F Nouailhat, J C Kaplan, Y Giudicelli, et al.

Human Genetics|July 7, 1976

Gene dosage effect in human triploid fibroblastsC Junien, H Rubinson, J C Dreyfus, et al.

Cancer Research|July 1, 1995

Seven megabase yeast artificial chromosome contig at region 11p15: identification of a yeast artificial chromosome spanning the breakpoint of a chromosomal translocation found in a case of Beckwith-Wiedemann syndromeM Negrini, S Sabbioni, M Ohta, et al.

Pageof 24

Showing results (101-110 of 232) with videos related to

Sort By:

Pageof 24

Human Genetics|June 1, 1997

alpha-satellite DNA methylation in normal individuals and in ICF patients: heterogeneous methylation of constitutive heterochromatin in adult and fetal tissuesP Miniou, M Jeanpierre, D Bourc'his, et al.

Human Genetics|March 1, 1989

Detection of 1q polysomy in interphase nuclei of human solid tumors with a biotinylated probeE Viegas-Péquignot, M Jeanpierre, A M Dutrillaux, et al.

Annales De Genetique|January 1, 1980

[Increase of LDH A and partial trisomy 11p (author's transl)]M O Rethoré, C Junien, A Aurias, et al.

DNA Research : an International Journal for Rapid Publication of Reports on Genes and Genomes|January 1, 1999

cDNA cloning, tissue distribution and chromosomal localization of the human ID4 geneM Rigolet, T Rich, M S Gross-Morand, et al.

Human Molecular Genetics|August 1, 1993

Myotonic dystrophy: absence of CTG enlarged transcript in congenital forms, and low expression of the normal alleleH Hofmann-Radvanyi, C Lavedan, J P Rabès, et al.

Human Genetics|January 1, 1984

Del11p13/nephroblastoma without aniridiaC Turleau, J de Grouchy, C Nihoul-Fékété, et al.

Human Genetics|January 19, 1978

Heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Algeria. Study in Northern Algeria with description of five new variantsM Benabadji, F Merad, M Benmoussa, et al.

Annales De Medecine Interne|November 1, 1977

[Generalized saturnine paralysis. Discovery of a double congenital disease: glucose-6-phosphate dehydrogenase deficiency (new variant) and distal tubular acidosis]F Nouailhat, J C Kaplan, Y Giudicelli, et al.

Human Genetics|July 7, 1976

Gene dosage effect in human triploid fibroblastsC Junien, H Rubinson, J C Dreyfus, et al.

Cancer Research|July 1, 1995

Seven megabase yeast artificial chromosome contig at region 11p15: identification of a yeast artificial chromosome spanning the breakpoint of a chromosomal translocation found in a case of Beckwith-Wiedemann syndromeM Negrini, S Sabbioni, M Ohta, et al.

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