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Chirurgie Pediatrique
|
January 1, 1990
[Prenatal diagnosis of sacro-coccygeal teratomas]
Y Heloury, P Vergnes, J M Classe, et al.
Annales De Genetique
|
January 1, 1983
[Localization of the LDHA-GST3-ESA4 synthetic group on human chromosome 11. Analyses of the classic man-rodent hybrids and of a new type (not adhering to the wall)]
V Laisney, Nguyen Van Cong, M S Gross, et al.
Nano Letters
|
July 24, 2013
Large-area free-standing ultrathin single-crystal silicon as processable materials
Shuang Wang, Benjamin D Weil, Yanbin Li, et al.
Archives Francaises De Pediatrie
|
December 1, 1979
[Monitoring of intracranial pressure in 2 severe cases of Reye's syndrome]
F Gold, A Chantepie, D Weil, et al.
The Journal of Biological Chemistry
|
June 25, 1988
Identification of a mutation that causes exon skipping during collagen pre-mRNA splicing in an Ehlers-Danlos syndrome variant
D Weil, M Bernard, N Combates, et al.
Human Genetics
|
January 1, 1983
Assignment of the human coproporphyrinogen oxidase to chromosome 9
B Grandchamp, D Weil, Y Nordmann, et al.
Reviews in Urology
|
September 21, 2006
Therapeutic Strategies for Localized Prostate Cancer II: Perineal Prostatectomy, X-Rays, Protons, Neutrons, and Combination Brachytherapy
M D Weil, A T Porter, D C Beyer, et al.
Cytogenetics and Cell Genetics
|
January 1, 1974
Proceedings: Assignment of the second locus of adenylate kinase to chromosome 1p: preliminary data
N Van Cong, R Rebourcet, D Weil, et al.
The EMBO Journal
|
June 1, 1989
A base substitution in the exon of a collagen gene causes alternative splicing and generates a structurally abnormal polypeptide in a patient with Ehlers-Danlos syndrome type VII
D Weil, M D'Alessio, F Ramirez, et al.
Human Genetics
|
October 1, 1979
[Localization of the gene for phosphoglycolate phosphatase (PGP) on the chromosome 16 by interspecific hybridization (author's transl)]
D Weil, N Van Cong, C Finaz, et al.
Page
of 21
Search research articles
Search
Showing results (131-140 of 203) with videos related to
Sort By:
Page
of 21
Chirurgie Pediatrique
|
January 1, 1990
[Prenatal diagnosis of sacro-coccygeal teratomas]
Y Heloury, P Vergnes, J M Classe, et al.
Annales De Genetique
|
January 1, 1983
[Localization of the LDHA-GST3-ESA4 synthetic group on human chromosome 11. Analyses of the classic man-rodent hybrids and of a new type (not adhering to the wall)]
V Laisney, Nguyen Van Cong, M S Gross, et al.
Nano Letters
|
July 24, 2013
Large-area free-standing ultrathin single-crystal silicon as processable materials
Shuang Wang, Benjamin D Weil, Yanbin Li, et al.
Archives Francaises De Pediatrie
|
December 1, 1979
[Monitoring of intracranial pressure in 2 severe cases of Reye's syndrome]
F Gold, A Chantepie, D Weil, et al.
The Journal of Biological Chemistry
|
June 25, 1988
Identification of a mutation that causes exon skipping during collagen pre-mRNA splicing in an Ehlers-Danlos syndrome variant
D Weil, M Bernard, N Combates, et al.
Human Genetics
|
January 1, 1983
Assignment of the human coproporphyrinogen oxidase to chromosome 9
B Grandchamp, D Weil, Y Nordmann, et al.
Reviews in Urology
|
September 21, 2006
Therapeutic Strategies for Localized Prostate Cancer II: Perineal Prostatectomy, X-Rays, Protons, Neutrons, and Combination Brachytherapy
M D Weil, A T Porter, D C Beyer, et al.
Cytogenetics and Cell Genetics
|
January 1, 1974
Proceedings: Assignment of the second locus of adenylate kinase to chromosome 1p: preliminary data
N Van Cong, R Rebourcet, D Weil, et al.
The EMBO Journal
|
June 1, 1989
A base substitution in the exon of a collagen gene causes alternative splicing and generates a structurally abnormal polypeptide in a patient with Ehlers-Danlos syndrome type VII
D Weil, M D'Alessio, F Ramirez, et al.
Human Genetics
|
October 1, 1979
[Localization of the gene for phosphoglycolate phosphatase (PGP) on the chromosome 16 by interspecific hybridization (author's transl)]
D Weil, N Van Cong, C Finaz, et al.
Page
of 21