M Jeanpierre|C Junien - JoVE Visualize

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Revue Des Maladies Respiratoires|January 1, 1991

[Tracheo-bronchial granular cell tumors. Apropos of 4 cases]F Blanc-Jouvan, E Brambilla, A Bosseray, et al.

The Journal of Clinical Investigation|January 1, 1991

Anderson's disease: genetic exclusion of the apolipoprotein-B gene in two familiesM Pessah, P Benlian, I Beucler, et al.

Human Genetics|January 1, 1981

Retinoblastoma-del(13q14): report of two patients, one with a trisomic sib due to maternal insertion. Gene-dosage effect for esterase DH Rivera, C Turleau, J de Grouchy, et al.

Nucleic Acids Research|January 1, 1997

Software and database for the analysis of mutations in the human LDL receptor geneM Varret, J P Rabès, G Collod-Béroud, et al.

Bulletin Du Cancer|January 1, 1991

[Antioncogenes: models for tumors in children]C Junien, I Henry, C Jeanpierre, et al.

Journal of Medical Genetics|February 1, 1991

Prenatal diagnosis of myotonic dystrophy using closely linked flanking markersC Lavedan, H Hofmann, P Shelbourne, et al.

Annales De Genetique|June 1, 1975

Partial deletion of the short arm of chromosome 12(p11; p13). Report of a caseR Tenconi, C Baccichetti, F Anglani, et al.

Cytogenetics and Cell Genetics|January 1, 1993

Specific induction of uncoiling and recombination by azacytidine in classical satellite-containing constitutive heterochromatinN Kokalj-Vokac, A Almeida, E Viegas-Péquignot, et al.

Human Genetics|January 1, 1985

The isolation, characterisation, and chromosomal assignment of the gene for human 3-hydroxy-3-methylglutaryl coenzyme A reductase, (HMG-CoA reductase)S E Humphries, F Tata, I Henry, et al.

Annales De Genetique|January 1, 1980

[Sesquialter dosage effect of erythrocytic and leucocytic nucleoside phosphorylase in two patients with proximal trisomy 14q (author's transl)]C Junien, J C Kaplan, O Raoul, et al.

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Revue Des Maladies Respiratoires|January 1, 1991

[Tracheo-bronchial granular cell tumors. Apropos of 4 cases]F Blanc-Jouvan, E Brambilla, A Bosseray, et al.

The Journal of Clinical Investigation|January 1, 1991

Anderson's disease: genetic exclusion of the apolipoprotein-B gene in two familiesM Pessah, P Benlian, I Beucler, et al.

Human Genetics|January 1, 1981

Retinoblastoma-del(13q14): report of two patients, one with a trisomic sib due to maternal insertion. Gene-dosage effect for esterase DH Rivera, C Turleau, J de Grouchy, et al.

Nucleic Acids Research|January 1, 1997

Software and database for the analysis of mutations in the human LDL receptor geneM Varret, J P Rabès, G Collod-Béroud, et al.

Bulletin Du Cancer|January 1, 1991

[Antioncogenes: models for tumors in children]C Junien, I Henry, C Jeanpierre, et al.

Journal of Medical Genetics|February 1, 1991

Prenatal diagnosis of myotonic dystrophy using closely linked flanking markersC Lavedan, H Hofmann, P Shelbourne, et al.

Annales De Genetique|June 1, 1975

Partial deletion of the short arm of chromosome 12(p11; p13). Report of a caseR Tenconi, C Baccichetti, F Anglani, et al.

Cytogenetics and Cell Genetics|January 1, 1993

Specific induction of uncoiling and recombination by azacytidine in classical satellite-containing constitutive heterochromatinN Kokalj-Vokac, A Almeida, E Viegas-Péquignot, et al.

Human Genetics|January 1, 1985

The isolation, characterisation, and chromosomal assignment of the gene for human 3-hydroxy-3-methylglutaryl coenzyme A reductase, (HMG-CoA reductase)S E Humphries, F Tata, I Henry, et al.

Annales De Genetique|January 1, 1980

[Sesquialter dosage effect of erythrocytic and leucocytic nucleoside phosphorylase in two patients with proximal trisomy 14q (author's transl)]C Junien, J C Kaplan, O Raoul, et al.

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