COURS DE MECANIQUES DES MILIEUX CONTINUS.

Por MANDEL J.
Publicado em S1966

Comparative Frequency of Fragile-X (FMR1) and Creatine Transporter (SLC6A8) Mutations in X-Linked Mental Retardation

Por Mandel, J. L.
Publicado em 2004

Mortality of employees of a perfluorooctanesulphonyl fluoride manufacturing facility

Por Alexander, B, Olsen, G, Burris, J, Mandel, J, Mandel, J
Publicado em 2003

DNA methylation: organ specific variations in the methylation pattern within and around ovalbumin and other chicken genes.

Por Mandel, J L, Chambon, P
Publicado em 1979

The glyceraldehyde 3 phosphate dehydrogenase gene family: structure of a human cDNA and of an X chromosome linked pseudogene; amazing complexity of the gene family in mouse.

Por Hanauer, A, Mandel, J L
Publicado em 1984

Selection of elderly controls using random digit dialing.

Por Olsen, G W, Mandel, J S
Publicado em 1988

ON THE CARBOHYDRATE GROUP IN THE NUCLEOPROTEID OF THE SPLEEN

Por Levene, P. A., Mandel, J. A.
Publicado em 1906

A 230kb cosmid walk in the Duchenne muscular dystrophy gene: detection of a conserved sequence and of a possible deletion prone region.

Por Heilig, R, Lemaire, C, Mandel, J L
Publicado em 1987

Nucleotide sequence of chicken dystrophin cDNA.

Por Lemaire, C, Heilig, R, Mandel, J L
Publicado em 1988

DNA methylation: correlation with DNase I sensitivity of chicken ovalbumin and conalbumin chromatin.

Por Kuo, M T, Mandel, J L, Chambon, P
Publicado em 1979

The chicken dystrophin cDNA: striking conservation of the C-terminal coding and 3' untranslated regions between man and chicken.

Por Lemaire, C, Heilig, R, Mandel, J L
Publicado em 1988

Instability of CAG repeats in Huntington's disease: relation to parental transmission and age of onset.

Por Trottier, Y, Biancalana, V, Mandel, J L
Publicado em 1994

Presence of a TaqI polymorphism in the human glutamate dehydrogenase (GLUD) gene on chromosome 10.

Por Hanauer, A, Mattei, M G, Mandel, J L
Publicado em 1987

Adenovirus as an expression vector in muscle cells in vivo.

Por Quantin, B, Perricaudet, L D, Tajbakhsh, S, Mandel, J L
Publicado em 1992

A DNA fragment from the human X chromosome short arm which detects a partially homologous sequence on the Y chromosomes long arm.

Por Koenig, M, Camerino, G, Heilig, R, Mandel, J L
Publicado em 1984

The ovalbumin gene family: complete sequence and structure of the Y gene.

Por Heilig, R, Muraskowsky, R, Kloepfer, C, Mandel, J L
Publicado em 1982

Repetitive satellite-like sequences are present within or upstream from 3 avian protein-coding genes.

Por Maroteaux, L, Heilig, R, Dupret, D, Mandel, J L
Publicado em 1983

A PstI RFLP for the human retinoic acid receptor in 17q21.

Por Arveiler, B, Petkovich, M, Mandel, J L, Chambon, P
Publicado em 1988

An XmnI RFLP at the subtelomeric Xp locus DXS31 [HGM7, LA, 1985]

Por Wrogemann, K, Koenig, M, Alembik, Y, Mandel, J L
Publicado em 1986

Selection in blood cells from female carriers of the fragile X syndrome: inverse correlation between age and proportion of active X chromosomes carrying the full mutation.

Por Rousseau, F, Heitz, D, Oberlé, I, Mandel, J L
Publicado em 1991