Exon trapping/amplification was used to clone portions of genes from the Down syndrome critical region (DSCR) of human chromosome 21q22. Two trapped sequences showed complete homology with nucleotide sequence D23672 of Genbank which corresponds to the gene for the human holocarboxylase synthetase (HCS) that was previously assigned to chromosome 21. We precisely mapped this gene to the DSCR by somatic cell hybrids, chromosome 21-specific YACs, and hybridization to chromosome 21-specific cosmids; it localizes to YACs 745H11 and 230E8 of the Chumakov et al. (Nature 359:380, 1992) YAC contig in a region of less that one megabase between markers D21S333 and D21S267. This HCS gene may contribute in a gene dosage-dependent manner to the phenotype ...
To help in isolating the genes involved in Down syndrome, we sought CpG islands in 4 Mb cosmid/PAC c...
Introduction: A \u201eDown Syndrome critical region\u201c (DSCR) sufficient to induce the most const...
Exon amplification has been applied to a 2.5 Mb region of chromosome 21 that has been associated wit...
Exon trapping was used to clone portions of genes from the Down syndrome critical region (DSCR) of h...
The region surrounding D21S55 in band 21q22 of human chromosome 21 has been implicated in the etiolo...
Down syndrome (DS), caused by the presence of an extra copy of human chromosome 21 (HC21), is the mo...
The Down syndrome (DS) region has been defined by analyses of partial trisomy 21. The 2.5-Mb region ...
Down syndrome (DS), caused by the presence of an extra copy of human chromosome 21 (HC21), is the mo...
A human genomic DNA fragment, pAM37 (HGM8; D21S22), was mapped to chromosome 21q2.1-q2.21 by in situ...
A human genomic DNA fragment, pAM37 (HGM8; D21S22), was mapped to chromosome 21q2.1-q2.21 by in situ...
A human genomic DNA fragment, pAM37 (HGM8; D21S22), was mapped to chromosome 21q2.1-q2.21 by in situ...
A human genomic DNA fragment, pAM37 (HGM8; D21S22), was mapped to chromosome 21q2.1-q2.21 by in situ...
To contribute to the development of the transcript map of human chromosome 21 and to the understandi...
Introduction: A „Down Syndrome critical region“ (DSCR) sufficient to induce the most constant pheno...
Introduction: A „Down Syndrome critical region“ (DSCR) sufficient to induce the most constant pheno...
To help in isolating the genes involved in Down syndrome, we sought CpG islands in 4 Mb cosmid/PAC c...
Introduction: A \u201eDown Syndrome critical region\u201c (DSCR) sufficient to induce the most const...
Exon amplification has been applied to a 2.5 Mb region of chromosome 21 that has been associated wit...
Exon trapping was used to clone portions of genes from the Down syndrome critical region (DSCR) of h...
The region surrounding D21S55 in band 21q22 of human chromosome 21 has been implicated in the etiolo...
Down syndrome (DS), caused by the presence of an extra copy of human chromosome 21 (HC21), is the mo...
The Down syndrome (DS) region has been defined by analyses of partial trisomy 21. The 2.5-Mb region ...
Down syndrome (DS), caused by the presence of an extra copy of human chromosome 21 (HC21), is the mo...
A human genomic DNA fragment, pAM37 (HGM8; D21S22), was mapped to chromosome 21q2.1-q2.21 by in situ...
A human genomic DNA fragment, pAM37 (HGM8; D21S22), was mapped to chromosome 21q2.1-q2.21 by in situ...
A human genomic DNA fragment, pAM37 (HGM8; D21S22), was mapped to chromosome 21q2.1-q2.21 by in situ...
A human genomic DNA fragment, pAM37 (HGM8; D21S22), was mapped to chromosome 21q2.1-q2.21 by in situ...
To contribute to the development of the transcript map of human chromosome 21 and to the understandi...
Introduction: A „Down Syndrome critical region“ (DSCR) sufficient to induce the most constant pheno...
Introduction: A „Down Syndrome critical region“ (DSCR) sufficient to induce the most constant pheno...
To help in isolating the genes involved in Down syndrome, we sought CpG islands in 4 Mb cosmid/PAC c...
Introduction: A \u201eDown Syndrome critical region\u201c (DSCR) sufficient to induce the most const...
Exon amplification has been applied to a 2.5 Mb region of chromosome 21 that has been associated wit...