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D Weil

Showing results (151-160 of 203) with videos related to

Pageof 21
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Human Genetics|May 1, 1986
The pro alpha 2(V) collagen gene (COL5A2) maps to 2q14----2q32, syntenic to the pro alpha 1 (III) collagen locus (COL3A1)C Huerre-Jeanpierre, I Henry, M Bernard, et al.
Human Molecular Genetics|September 25, 1997
Abnormal XY interchange between a novel isolated protein kinase gene, PRKY, and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY femalesK Schiebel, M Winkelmann, A Mertz, et al.
Mycopathologia|April 3, 2017
Paecilomyces variotii Fungemia in a Patient with Lymphoma Needing Liver TransplantA P Bellanger, J P Cervoni, J F Faucher, et al.
Nature|June 10, 1998
Connexin 26 gene linked to a dominant deafnessF Denoyelle, G Lina-Granade, H Plauchu, et al.
Human Molecular Genetics|February 9, 1999
An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21M Mustapha, D Weil, S Chardenoux, et al.
Annals of Human Genetics|July 1, 1980
Assignment of the gene for F-type phosphofructokinase to human chromosome 10 by somatic cell hybridization and specific immunoprecipitationD Weil, D Cottreau, Nguyen Van Cong, et al.
Revue De Chirurgie Orthopedique Et Reparatrice De L'Appareil Moteur|January 1, 1988
[The use of enoxaparine in preventing deep venous thrombosis following total hip prosthesis. Randomized multicenter prospective trial]A Planes, N Vochelle, F Mazas, et al.
Annals of Human Genetics|July 1, 1985
The structural gene for aldolase B (ALDB) maps to 9q13----32I Henry, P Gallano, C Besmond, et al.
Human Genetics|January 1, 1984
Assignment of the gene for uroporphyrinogen decarboxylase to human chromosome 1 by somatic cell hybridization and specific enzyme immunoassayH de Verneuil, B Grandchamp, C Foubert, et al.
Annales De Genetique|December 1, 1972
[Probable existence of a 2d AK locus linked with the PGM 1 -peptidase C group]Van-Cong-Nguyen, C Billardon, R Rebourcet, et al.
Pageof 21

Showing results (151-160 of 203) with videos related to

Sort By:
Pageof 21
Human Genetics|May 1, 1986
The pro alpha 2(V) collagen gene (COL5A2) maps to 2q14----2q32, syntenic to the pro alpha 1 (III) collagen locus (COL3A1)C Huerre-Jeanpierre, I Henry, M Bernard, et al.
Human Molecular Genetics|September 25, 1997
Abnormal XY interchange between a novel isolated protein kinase gene, PRKY, and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY femalesK Schiebel, M Winkelmann, A Mertz, et al.
Mycopathologia|April 3, 2017
Paecilomyces variotii Fungemia in a Patient with Lymphoma Needing Liver TransplantA P Bellanger, J P Cervoni, J F Faucher, et al.
Nature|June 10, 1998
Connexin 26 gene linked to a dominant deafnessF Denoyelle, G Lina-Granade, H Plauchu, et al.
Human Molecular Genetics|February 9, 1999
An alpha-tectorin gene defect causes a newly identified autosomal recessive form of sensorineural pre-lingual non-syndromic deafness, DFNB21M Mustapha, D Weil, S Chardenoux, et al.
Annals of Human Genetics|July 1, 1980
Assignment of the gene for F-type phosphofructokinase to human chromosome 10 by somatic cell hybridization and specific immunoprecipitationD Weil, D Cottreau, Nguyen Van Cong, et al.
Revue De Chirurgie Orthopedique Et Reparatrice De L'Appareil Moteur|January 1, 1988
[The use of enoxaparine in preventing deep venous thrombosis following total hip prosthesis. Randomized multicenter prospective trial]A Planes, N Vochelle, F Mazas, et al.
Annals of Human Genetics|July 1, 1985
The structural gene for aldolase B (ALDB) maps to 9q13----32I Henry, P Gallano, C Besmond, et al.
Human Genetics|January 1, 1984
Assignment of the gene for uroporphyrinogen decarboxylase to human chromosome 1 by somatic cell hybridization and specific enzyme immunoassayH de Verneuil, B Grandchamp, C Foubert, et al.
Annales De Genetique|December 1, 1972
[Probable existence of a 2d AK locus linked with the PGM 1 -peptidase C group]Van-Cong-Nguyen, C Billardon, R Rebourcet, et al.
Pageof 21