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de la CHAPELLE

Showing results (41-50 of 603) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1978
Multiple cytogenetic methods used to identify a new structural rearrangement of the human X chromosomeA de la Chapelle, P Grönman, S A Latt
Journal of Medical Genetics|November 2, 1999
Strategies for screening for hereditary non-polyposis colorectal cancerA Loukola, A de la Chapelle, L A Aaltonen
Scandinavian Journal of Haematology|August 1, 1976
Polyploidy of the bone marrowG H Borgström, P Vuopio, A De la Chapelle
Genomics|March 1, 1991
Refined localization of the gene causing X-linked juvenile retinoschisisT Alitalo, T A Kruse, A de la Chapelle
Science (New York, N.Y.)|August 15, 1986
Chromosome Y-specific DNA is transferred to the short arm of X chromosome in human XX malesM Andersson, D C Page, A de la Chapelle
Cytogenetics and Cell Genetics|January 1, 1989
Determination of the breakpoints of 1;7 translocations in myelodysplastic syndrome by in situ hybridization using chromosome-specific alpha satellite DNA from human chromosomes 1 and 7T Alitalo, H F Willard, A de la Chapelle
International Journal of Cancer|March 18, 2003
Hypermethylation, but not LOH, is associated with the low expression of MT1G and CRABP1 in papillary thyroid carcinomaYing Huang, Albert de la Chapelle, Natalia S Pellegata
Clinical Genetics|September 1, 1990
Hemophilia B: diagnostic value of RFLP analysis in 19 of the 20 known Finnish familiesA E Lehesjoki, V Rasi, A de la Chapelle
Proceedings of the National Academy of Sciences of the United States of America|May 15, 1993
Truncated erythropoietin receptor causes dominantly inherited benign human erythrocytosisA de la Chapelle, A L Träskelin, E Juvonen
Mutation Research|September 1, 1990
Assessment by Southern blot analysis of UV-induced damage and repair in human immunoglobulin genesM S Bianchi, N O Bianchi, A de la Chapelle
Pageof 61

Showing results (41-50 of 603) with videos related to

Sort By:
Pageof 61
Cytogenetics and Cell Genetics|January 1, 1978
Multiple cytogenetic methods used to identify a new structural rearrangement of the human X chromosomeA de la Chapelle, P Grönman, S A Latt
Journal of Medical Genetics|November 2, 1999
Strategies for screening for hereditary non-polyposis colorectal cancerA Loukola, A de la Chapelle, L A Aaltonen
Scandinavian Journal of Haematology|August 1, 1976
Polyploidy of the bone marrowG H Borgström, P Vuopio, A De la Chapelle
Genomics|March 1, 1991
Refined localization of the gene causing X-linked juvenile retinoschisisT Alitalo, T A Kruse, A de la Chapelle
Science (New York, N.Y.)|August 15, 1986
Chromosome Y-specific DNA is transferred to the short arm of X chromosome in human XX malesM Andersson, D C Page, A de la Chapelle
Cytogenetics and Cell Genetics|January 1, 1989
Determination of the breakpoints of 1;7 translocations in myelodysplastic syndrome by in situ hybridization using chromosome-specific alpha satellite DNA from human chromosomes 1 and 7T Alitalo, H F Willard, A de la Chapelle
International Journal of Cancer|March 18, 2003
Hypermethylation, but not LOH, is associated with the low expression of MT1G and CRABP1 in papillary thyroid carcinomaYing Huang, Albert de la Chapelle, Natalia S Pellegata
Clinical Genetics|September 1, 1990
Hemophilia B: diagnostic value of RFLP analysis in 19 of the 20 known Finnish familiesA E Lehesjoki, V Rasi, A de la Chapelle
Proceedings of the National Academy of Sciences of the United States of America|May 15, 1993
Truncated erythropoietin receptor causes dominantly inherited benign human erythrocytosisA de la Chapelle, A L Träskelin, E Juvonen
Mutation Research|September 1, 1990
Assessment by Southern blot analysis of UV-induced damage and repair in human immunoglobulin genesM S Bianchi, N O Bianchi, A de la Chapelle
Pageof 61