| | Title | Authors / Editors | Date |
|
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:8845 |
What is expanded in progressive myoclonus epilepsy? |
Lalioti, M. D.; Scott, Hamish Steele; Antonarakis, Stylianos |
1997 |
|
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:8699 |
Transcriptional map of the 2.5-Mb CBR-ERG region of chromosome 21 involved in Down syndrome |
Dahmane, N.; Ghezala, G. A.; Gosset, P.; Chamoun, Z.; ... Delabar, J. M. |
1998 |
|
unige:9153 |
The SH3D1A gene maps to human chromosome 21q22.1-->q22.2 |
Chen, H.; Antonarakis, Stylianos |
1997 |
|
unige:9106 |
The human lanosterol synthase gene maps to chromosome 21q22.3 |
Young, M.; Chen, H.; Lalioti, M. D.; 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:8796 |
The DNA sequence of human chromosome 21 |
Hattori, M. |
2000 |
|
unige:8675 |
Single-minded and Down syndrome? |
Chen, H.; Chrast, R.; Rossier, Colette; Gos, A.; ... Minoshima, S. |
1995 |
|
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:9259 |
Refined genetic mapping of the autosomal recessive non-syndromic deafness locus DFNB8 on human chromosome 21q22.3 |
Scott, Hamish Steele; Antonarakis, Stylianos; Mittaz, L.; Lalioti, M. D.; ... Gal, A. |
2000 |
|
unige:8918 |
Positional cloning of the APECED gene |
Nagamine, K.; Peterson, P.; Scott, Hamish Steele; Kudoh, J.; ... Shimizu, N. |
1997 |
|
unige:8644 |
Normal phenotype with paternal uniparental isodisomy for chromosome 21 |
Blouin, Jean-Louis; Avramopoulos, D.; Pangalos, C.; Antonarakis, Stylianos |
1993 |
|
unige:8988 |
Nineteen additional unpredicted transcripts from human chromosome 21 |
Reymond, Alexandre; Camargo, A. A.; Deutsch, Samuel; Stevenson, B. J.; ... Antonarakis, Stylianos |
2002 |
|
unige:8969 |
Natural gene-expression variation in Down syndrome modulates the outcome of gene-dosage imbalance |
Prandini, Paola; Deutsch, Samuel; Lyle, Robert; Gagnebin, Maryline; ... Antonarakis, Stylianos |
2007 |
|
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: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:8672 |
Localization of a human homolog of the mouse Tiam-1 gene to chromosome 21q22.1 |
Chen, H.; Antonarakis, Stylianos |
1995 |
|
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 |
|
unige:8673 |
Localisation of a human homologue of the Drosophila mnb and rat Dyrk genes to chromosome 21q22.2 |
Chen, H.; Antonarakis, Stylianos |
1997 |
Chromosomes, human, pair 21
add all
remove all
