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 TitleAuthors / EditorsDate
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Schizophrenia susceptibility and chromosome 6p24-22 Antonarakis, Stylianos; Blouin, Jean-Louis; Pulver, A. E.; Wolyniec, P.; ... Dombroski, B. 1995
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Factor VIII gene inversions in severe hemophilia A: results of an international consortium study Antonarakis, Stylianos 1995
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Targeted disruption of the mouse factor VIII gene produces a model of haemophilia A Bi, L.; Lawler, A. M.; Antonarakis, Stylianos; High, K. A.; ... Kazazian, H. H. 1995
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A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombination Blouin, Jean-Louis; Christie, D. H.; Gos, A.; Lynn, A.; ... Antonarakis, Stylianos 1995
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Localization of a human homolog of the mouse Tiam-1 gene to chromosome 21q22.1 Chen, H.; Antonarakis, Stylianos 1995
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Single-minded and Down syndrome? Chen, H.; Chrast, R.; Rossier, Colette; Gos, A.; ... Minoshima, S. 1995
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Cloning of the cDNA for the human ATP synthase OSCP subunit (ATP5O) by exon trapping and mapping to chromosome 21q22.1-q22.2 Chen, H.; Morris, Michael Andréw; Rossier, Colette; Blouin, Jean-Louis; Antonarakis, Stylianos 1995
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Mapping of the human transcription factor GABPA (E4TF1-60) gene to chromosome 21 Chrast, R.; Chen, H.; Morris, Michael Andréw; Antonarakis, Stylianos 1995
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Two-dimensional electrophoresis southern transfer method for detecting human genome variability using a LINE-1 sequence probe Nakashima, H.; Yi, M.; Ichikawa, N.; LeBlond, G. F.; ... Ts'o, P. O. 1995
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Exon skipping associated with A-->G transition at +4 of the IVS33 splice donor site of the neurofibromatosis type 1 (NF1) gene Hutter, P.; Antonarakis, Stylianos; Delozier-Blanchet, C. D.; Morris, Michael Andréw 1994
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Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives Pulver, A. E.; Nestadt, G.; Goldberg, R.; Shprintzen, R. J.; ... Housman, D. 1994
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Dinucleotide repeat polymorphism within ERCC5 gene Samec, S.; Clarkson, S. G.; Blaschak, J.; Chakravarti, A.; ... Antonarakis, Stylianos 1994
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Homologous loci DXYS156X and DXYS156Y contain a polymorphic pentanucleotide repeat (TAAAA)n and map to human X and Y chromosomes Chen, H.; Lowther, W.; Avramopoulos, D.; Antonarakis, Stylianos 1994
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Discussion on mutation nomenclature Cotton, R. G. H.; Kazazian, H. H.; Antonarakis, Stylianos; McKusick, V. A. 1994
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Biparental inheritance of chromosome 21 polymorphic markers indicates that some Robertsonian translocations t(21;21) occur postzygotically Blouin, Jean-Louis; Binkert, F.; Antonarakis, Stylianos 1994
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Genome linkage scanning: systematic or intelligent? Antonarakis, Stylianos 1994
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Understanding the mechanism(s) of mosaic trisomy 21 by using DNA polymorphism analysis Pangalos, C.; Avramopoulos, D.; Blouin, Jean-Louis; Raoul, O.; ... Antonarakis, Stylianos 1994
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Human chromosome 21: genome mapping and exploration, circa 1993 Antonarakis, Stylianos 1993
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Report of the Fourth International Workshop on Human Chromosome 21 Delabar, J. M.; Creau, N.; Sinet, P. M.; Ritter, O.; ... Patterson, D. 1993
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Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A Lakich, D.; Kazazian, H. H.; Antonarakis, Stylianos; Gitschier, J. 1993
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