| Title | Authors / Editors | Date |
unige:9164 |
Report of the Fourth International Workshop on Human Chromosome 21 |
Delabar, J. M.; Creau, N.; Sinet, P. M.; Ritter, O.; ... Patterson, D. |
1993 |
unige:8644 |
Normal phenotype with paternal uniparental isodisomy for chromosome 21 |
Blouin, Jean-Louis; Avramopoulos, D.; Pangalos, C.; Antonarakis, Stylianos |
1993 |
unige:8840 |
Inversions disrupting the factor VIII gene are a common cause of severe haemophilia A |
Lakich, D.; Kazazian, H. H.; Antonarakis, Stylianos; Gitschier, J. |
1993 |
unige:9127 |
Human chromosome 21: genome mapping and exploration, circa 1993 |
Antonarakis, Stylianos |
1993 |
unige:8597 |
Genome linkage scanning: systematic or intelligent? |
Antonarakis, Stylianos |
1994 |
unige:8950 |
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 |
unige:9132 |
Discussion on mutation nomenclature |
Cotton, R. G. H.; Kazazian, H. H.; Antonarakis, Stylianos; McKusick, V. A. |
1994 |
unige:9144 |
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 |
unige:9154 |
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 |
unige:9205 |
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 |
unige:9247 |
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 |
unige:9257 |
Dinucleotide repeat polymorphism within ERCC5 gene |
Samec, S.; Clarkson, S. G.; Blaschak, J.; Chakravarti, A.; ... Antonarakis, Stylianos |
1994 |
unige:8614 |
Factor VIII gene inversions in severe hemophilia A: results of an international consortium study |
Antonarakis, Stylianos |
1995 |
unige:8672 |
Localization of a human homolog of the mouse Tiam-1 gene to chromosome 21q22.1 |
Chen, H.; Antonarakis, Stylianos |
1995 |
unige:8678 |
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 |
unige:8684 |
Mapping of the human transcription factor GABPA (E4TF1-60) gene to chromosome 21 |
Chrast, R.; Chen, H.; Morris, Michael Andréw; Antonarakis, Stylianos |
1995 |
unige:8606 |
Schizophrenia susceptibility and chromosome 6p24-22 |
Antonarakis, Stylianos; Blouin, Jean-Louis; Pulver, A. E.; Wolyniec, P.; ... Dombroski, B. |
1995 |
unige:8641 |
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 |
unige:8645 |
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 |
unige:8675 |
Single-minded and Down syndrome? |
Chen, H.; Chrast, R.; Rossier, Colette; Gos, A.; ... Minoshima, S. |
1995 |