| | 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:9127 |
Human chromosome 21: genome mapping and exploration, circa 1993 |
Antonarakis, Stylianos |
1993 |
|
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: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: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 |
|
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:8672 |
Localization of a human homolog of the mouse Tiam-1 gene to chromosome 21q22.1 |
Chen, H.; Antonarakis, Stylianos |
1995 |
|
unige:8675 |
Single-minded and Down syndrome? |
Chen, H.; Chrast, R.; Rossier, Colette; Gos, A.; ... Minoshima, S. |
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:9106 |
The human lanosterol synthase gene maps to chromosome 21q22.3 |
Young, M.; Chen, H.; Lalioti, M. D.; Antonarakis, Stylianos |
1996 |
|
unige:9032 |
A gene which causes severe ocular alterations and occipital encephalocele (Knobloch syndrome) is mapped to 21q22.3 |
Sertie, A. L.; Quimby, M.; Moreira, E. S.; Murray, J.; ... Passos-Bueno, M. R. |
1996 |
|
unige:8842 |
Cloning the cDNA of human PWP2, which encodes a protein with WD repeats and maps to 21q22.3 |
Lalioti, M. D.; Chen, H.; Rossier, Colette; Shafaatian, R.; ... Antonarakis, Stylianos |
1996 |
|
unige:8843 |
The gene for human U2 snRNP auxiliary factor small 35-kDa subunit (U2AF1) maps to the progressive myoclonus epilepsy (EPM1) critical region on chromosome 21q22.3 |
Lalioti, M. D.; Gos, A.; Green, M. R.; Rossier, Colette; ... Antonarakis, Stylianos |
1996 |
|
unige:8917 |
YAC and cosmid FISH mapping of an unbalanced chromosomal translocation causing partial trisomy 21 and Down syndrome |
Nadal, M.; Mila, M.; Pritchard, M.; Mur, A.; ... Estivill, X. |
1996 |
|
unige:8648 |
Mapping of the gene for the p60 subunit of the human chromatin assembly factor (CAF1A) to the Down syndrome region of chromosome 21 |
Blouin, Jean-Louis; Duriaux Sail, Geneviève; Chen, H.; Gos, A.; ... Antonarakis, Stylianos |
1996 |
|
unige:8674 |
Cloning of the cDNA for a human homolog of the rat PEP-19 gene and mapping to chromosome 21q22.2-q22.3 |
Chen, H.; Bouras, Constantin; Antonarakis, Stylianos |
1996 |
|
unige:8676 |
Cloning of 559 potential exons of genes of human chromosome 21 by exon trapping |
Chen, H.; Chrast, R.; Rossier, Colette; Morris, Michael Andréw; ... Antonarakis, Stylianos |
1996 |
|
unige:8677 |
Localization of a human homolog of the mouse pericentrin gene (PCNT) to chromosome 21qter |
Chen, H.; Gos, A.; Morris, Michael Andréw; Antonarakis, Stylianos |
1996 |
Chromosomes, human, pair 21
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