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In situ hybridization, fluorescence
 
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 TitleAuthors / EditorsDate
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 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
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 Genotype and phenotype analysis at the 22q11 schizophrenia susceptibility locus Karayiorgou, M.; Gogos, J. A.; Galke, B. L.; Jeffery, J. A.; ... Pulver, A. E. 1996
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 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
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 Localization of a human homolog of the mouse pericentrin gene (PCNT) to chromosome 21qter Chen, H.; Gos, A.; Morris, Michael Andréw; Antonarakis, Stylianos 1996
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 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
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 Familial translocation t(Y;15)(q12;p11) and de novo deletion of the Prader-Willi syndrome (PWS) critical region on 15q11-q13 Eliez, Stéphan; Morris, Michael Andréw; Dahoun-Hadorn, S.; DeLozier-Blanchet, C. D.; ... Antonarakis, Stylianos 1997
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 Trisomy 1q generating translocations in Wilms tumor Betts, D R; Ilg, E C; Ozsahin, Ayse Hulya; von der Weid, N; Niggli, F K 1999
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 Assignment of the human dynein heavy chain gene DNAH17L to human chromosome 17p12 by in situ hybridization and radiation hybrid mapping Bartoloni, Lucia; Blouin, Jean-Louis; Sainsbury, A. J.; Gos, A.; ... Antonarakis, Stylianos 1999
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 A high-resolution physical map of human chromosome 21p using yeast artificial chromosomes Wang, S. Y.; Cruts, M.; Del-Favero, J.; Zhang, Y.; ... van Broeckhoven, C. 1999
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 A testis-specific gene, TPTE, encodes a putative transmembrane tyrosine phosphatase and maps to the pericentromeric region of human chromosomes 21 and 13, and to chromosomes 15, 22, and Y Chen, H.; Rossier, Colette; Morris, Michael Andréw; Scott, Hamish Steele; ... Antonarakis, Stylianos 1999
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 FISH for Y chromosome in women with primary biliary cirrhosis: lack of evidence for leukocyte microchimerism Rubbia-Brandt, Laura; Philippeaux, Marie-Marthe; Chavez, S; Mentha, Gilles; ... Hadengue, Antoine 1999
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 A case of 45,X Turner syndrome with spontaneous ovulation proven by ultrasonography Giacobino, Ariane; Dahoun, Sophie; Sizonenko, Pierre-Claude; Stalberg, Anna-Maria; ... Campana, Aldo 2000
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 Genomic structure of a copy of the human TPTE gene which encompasses 87 kb on the short arm of chromosome 21 Guipponi, Michel; Yaspo, M. L.; Riesselman, L.; Chen, H.; ... Antonarakis, Stylianos 2000
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 Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness Scott, Hamish Steele; Kudoh, J.; Wattenhofer, M.; Shibuya, K.; ... Antonarakis, Stylianos 2001
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 Two regulatory levels of transcriptional gene silencing in Arabidopsis Mittelsten Scheid, Ortrun; Probst, Aline V.; Afsar, Karin; Paszkowski, Jerzy 2002
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 A t(2;8) balanced translocation with breakpoints near the human HOXD complex causes mesomelic dysplasia and vertebral defects Spitz, François; Montavon, Thomas; Monso-Hinard, Christine; Morris, Michael Andréw; ... Duboule, Denis 2002
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 Two means of transcriptional reactivation within heterochromatin Probst, Aline V.; Fransz, Paul F.; Paszkowski, Jerzy; Mittelsten Scheid, Ortrun 2003
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 The transcription factor RFX3 directs nodal cilium development and left-right asymmetry specification Bonnafe, E.; Touka, M.; Ait-Lounis, Aouatef; Baas, Dominique; ... Reith, Walter 2004
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 BRU1, a novel link between responses to DNA damage and epigenetic gene silencing in Arabidopsis Takeda, Shin; Tadele, Zerihun; Hofmann, Ingo; Probst, Aline V.; ... Paszkowski, Jerzy 2004
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 No association between DUP25 and anxiety disorders Henrichsen, C. N.; Delorme, Richard; Boucherie, Maria; Marelli, Dominique; ... Dahoun, Sophie 2004
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