L Bachner|J C Kaplan - JoVE Visualize

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Biochemical and Biophysical Research Communications|July 31, 1991

Illegitimate (or ectopic) transcription proceeds through the usual promotersJ Chelly, J P Hugnot, J P Concordet, et al.

Human Heredity|May 1, 1996

A splicing mutation in intron 16 of the cystic fibrosis transmembrane conductance regulator gene, associated with severe disease, is common on Reunion IslandT Bienvenu, F Cartault, F Lesure, et al.

Prenatal Diagnosis|January 13, 1999

Prenatal diagnosis of limb-girdle muscular dystrophy type 2CP Dinçer, F Piccolo, F Leturcq, et al.

Journal of Medical Genetics|April 1, 1994

Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north AfricaF el Kerch, A Sefiani, K Azibi, et al.

Nature Genetics|July 1, 1994

Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cenK Zerres, G Mücher, L Bachner, et al.

Human Molecular Genetics|September 1, 1993

Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12K Azibi, L Bachner, J S Beckmann, 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.

Nature|March 1, 1990

Dystrophin gene transcribed from different promoters in neuronal and glial cellsJ Chelly, G Hamard, A Koulakoff, et al.

The Journal of Biological Chemistry|May 25, 1992

Positive and negative regulatory DNA elements including a CCArGG box are involved in the cell type-specific expression of the human muscle dystrophin geneH Gilgenkrantz, J P Hugnot, M Lambert, et al.

Journal of Acquired Immune Deficiency Syndromes|January 1, 1990

Detection of HIV-1 DNA in crude cell lysates of peripheral blood mononuclear cells by the polymerase chain reaction and nonradioactive oligonucleotide probesB Conway, K E Adler, L J Bechtel, et al.

Pageof 19

Showing results (71-80 of 185) with videos related to

Sort By:

Pageof 19

Biochemical and Biophysical Research Communications|July 31, 1991

Illegitimate (or ectopic) transcription proceeds through the usual promotersJ Chelly, J P Hugnot, J P Concordet, et al.

Human Heredity|May 1, 1996

A splicing mutation in intron 16 of the cystic fibrosis transmembrane conductance regulator gene, associated with severe disease, is common on Reunion IslandT Bienvenu, F Cartault, F Lesure, et al.

Prenatal Diagnosis|January 13, 1999

Prenatal diagnosis of limb-girdle muscular dystrophy type 2CP Dinçer, F Piccolo, F Leturcq, et al.

Journal of Medical Genetics|April 1, 1994

Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north AfricaF el Kerch, A Sefiani, K Azibi, et al.

Nature Genetics|July 1, 1994

Mapping of the gene for autosomal recessive polycystic kidney disease (ARPKD) to chromosome 6p21-cenK Zerres, G Mücher, L Bachner, et al.

Human Molecular Genetics|September 1, 1993

Severe childhood autosomal recessive muscular dystrophy with the deficiency of the 50 kDa dystrophin-associated glycoprotein maps to chromosome 13q12K Azibi, L Bachner, J S Beckmann, 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.

Nature|March 1, 1990

Dystrophin gene transcribed from different promoters in neuronal and glial cellsJ Chelly, G Hamard, A Koulakoff, et al.

The Journal of Biological Chemistry|May 25, 1992

Positive and negative regulatory DNA elements including a CCArGG box are involved in the cell type-specific expression of the human muscle dystrophin geneH Gilgenkrantz, J P Hugnot, M Lambert, et al.

Journal of Acquired Immune Deficiency Syndromes|January 1, 1990

Detection of HIV-1 DNA in crude cell lysates of peripheral blood mononuclear cells by the polymerase chain reaction and nonradioactive oligonucleotide probesB Conway, K E Adler, L J Bechtel, et al.

Pageof 19