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Showing results (81-90 of 603) with videos related to

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Clinical Genetics|March 1, 1991
Hemophilia A: genetic prediction and linkage studies in all available families in FinlandA E Lehesjoki, P Sistonen, V Rasi, et al.
Journal of Medical Genetics|December 1, 1986
Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphismsM Lindlöf, H Kääriäinen, K E Davies, et al.
Sensors (Basel, Switzerland)|September 8, 2015
Enhanced Vibrational Spectroscopies as Tools for Small Molecule BiosensingSouhir Boujday, Marc Lamy de la Chapelle, Johannes Srajer, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|March 15, 2006
Hypermethylation of the MLH1 promoter with concomitant absence of transcript and protein occurs in small patches of crypt cells in unaffected mucosa from sporadic colorectal carcinomaGerard J Nuovo, Hidewaki Nakagawa, Kaisa Sotamaa, et al.
Cancer Genetics and Cytogenetics|March 1, 1984
Fourth International Workshop on Chromosomes in Leukemia 1982: Clinical significance of chromosomal abnormalities in acute nonlymphoblastic leukemiaC D Bloomfield, A Goldman, D Hassfeld, et al.
Biomedical Optics Express|May 14, 2013
Zirconia dental implants degradation by confocal Raman microspectroscopy: analytical simulation and experimentsNadia Djaker, Claudine Wulfman, Michaël Sadoun, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Chromosome 7 long-arm deletions in myeloid disorders: terminal DNA sequences are commonly conserved and breakpoints varyJ Kere, H Donis-Keller, T Ruutu, et al.
American Journal of Human Genetics|January 1, 1990
Molecular analysis of hemophilia A mutations in the Finnish populationB Levinson, A E Lehesjoki, A de la Chapelle, et al.
Seminars in Oncology|February 1, 1997
Clinical significance of cytogenetics in acute myeloid leukemiaK Mrózek, K Heinonen, A de la Chapelle, et al.
Acta Paediatrica Scandinavica|July 1, 1976
Primary hypothyroidism, growth hormone deficiency and congenital malformations in a child with the karyotype 46,XY,del(1)(q25q32)M Koivisto, H K Akerblom, M Remes, et al.
Pageof 61

Showing results (81-90 of 603) with videos related to

Sort By:
Pageof 61
Clinical Genetics|March 1, 1991
Hemophilia A: genetic prediction and linkage studies in all available families in FinlandA E Lehesjoki, P Sistonen, V Rasi, et al.
Journal of Medical Genetics|December 1, 1986
Carrier detection and prenatal diagnosis in X linked muscular dystrophy using restriction fragment length polymorphismsM Lindlöf, H Kääriäinen, K E Davies, et al.
Sensors (Basel, Switzerland)|September 8, 2015
Enhanced Vibrational Spectroscopies as Tools for Small Molecule BiosensingSouhir Boujday, Marc Lamy de la Chapelle, Johannes Srajer, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|March 15, 2006
Hypermethylation of the MLH1 promoter with concomitant absence of transcript and protein occurs in small patches of crypt cells in unaffected mucosa from sporadic colorectal carcinomaGerard J Nuovo, Hidewaki Nakagawa, Kaisa Sotamaa, et al.
Cancer Genetics and Cytogenetics|March 1, 1984
Fourth International Workshop on Chromosomes in Leukemia 1982: Clinical significance of chromosomal abnormalities in acute nonlymphoblastic leukemiaC D Bloomfield, A Goldman, D Hassfeld, et al.
Biomedical Optics Express|May 14, 2013
Zirconia dental implants degradation by confocal Raman microspectroscopy: analytical simulation and experimentsNadia Djaker, Claudine Wulfman, Michaël Sadoun, et al.
Cytogenetics and Cell Genetics|January 1, 1989
Chromosome 7 long-arm deletions in myeloid disorders: terminal DNA sequences are commonly conserved and breakpoints varyJ Kere, H Donis-Keller, T Ruutu, et al.
American Journal of Human Genetics|January 1, 1990
Molecular analysis of hemophilia A mutations in the Finnish populationB Levinson, A E Lehesjoki, A de la Chapelle, et al.
Seminars in Oncology|February 1, 1997
Clinical significance of cytogenetics in acute myeloid leukemiaK Mrózek, K Heinonen, A de la Chapelle, et al.
Acta Paediatrica Scandinavica|July 1, 1976
Primary hypothyroidism, growth hormone deficiency and congenital malformations in a child with the karyotype 46,XY,del(1)(q25q32)M Koivisto, H K Akerblom, M Remes, et al.
Pageof 61