| | Title | Authors / Editors | Date |
|
unige:9127 |
Human chromosome 21: genome mapping and exploration, circa 1993 |
Antonarakis, Stylianos |
1993 |
|
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: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:8644 |
Normal phenotype with paternal uniparental isodisomy for chromosome 21 |
Blouin, Jean-Louis; Avramopoulos, D.; Pangalos, C.; Antonarakis, Stylianos |
1993 |
|
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: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: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: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:9128 |
Molecular genetics of coagulation factor VIII gene and hemophilia A |
Antonarakis, Stylianos |
1995 |
|
unige:9130 |
Molecular etiology of factor VIII deficiency in hemophilia A |
Antonarakis, Stylianos; Kazazian, H. H.; Gitschier, J.; Hutter, P.; ... Morris, Michael Andréw |
1995 |
|
unige:9216 |
Localization of 102 exons to a 2.5 Mb region involved in Down syndrome |
Lucente, D.; Chen, H. M.; Shea, D.; Samec, S. N.; ... McCormick, M. K. |
1995 |
|
unige:9217 |
Characterization of cDNA clones containing CCA trinucleotide repeats derived from human brain |
Margolis, R. L.; Breschel, T. S.; Li, S. H.; Kidwai, A. S.; ... Ross, C. A. |
1995 |
|
unige:9262 |
The tetranucleotide repeat polymorphism D21S1245 demonstrates hypermutability in germline and somatic cells |
Talbot, C. C.; Avramopoulos, D.; Gerken, S.; Chakravarti, A.; ... Antonarakis, Stylianos |
1995 |
|
unige:9264 |
Characterization and chromosomal localization of a human P2X receptor from the urinary bladder |
Valera, S.; Talabot, F.; Evans, R. J.; Gos, A.; ... Buell, G. N. |
1995 |
|
unige:9213 |
Follow-up report of potential linkage for schizophrenia on chromosome 22q: Part 3 |
Lasseter, V. K.; Pulver, A. E.; Wolyniec, P. S.; Nestadt, G.; ... Kasch, L. |
1995 |
|
unige:9251 |
Duplication and loss of chromosome 21 in two children with Down syndrome and acute leukemia |
Rogan, P. K.; Close, P.; Blouin, Jean-Louis; Seip, J. R.; ... Antonarakis, Stylianos |
1995 |
Antonarakis, Stylianos
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