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21q22.2

A chromosome band present on 21q
National Institutes of Health

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5 relations
21qCBR3 wt AlleleChromosomesETS2 wt Allele

Papers overview

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Review
2013
Review
2013
Partial trisomy and tetrasomy of chromosome 21 without Down Syndrome phenotype and short overview of genotype-phenotype correlation. A case report.
AIMS Trisomy of chromosome 21 is associated with Down syndrome (DS) - the commonest genetic cause of mental retardation. We… 
Review
2006
Review
2006
Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32→qter) and partial monosomy 21q (21q22.2→qter)
To present the prenatal findings and molecular cytogenetic analyses of partial trisomy 12q and partial monosomy 21q, and a review… 
2005
2005
Clinical, cytogenetic, and molecular evaluation of a patient with partial trisomy 21 (21q11-q22) lacking the classical Down syndrome phenotype.
The clinical, cytogenetic, and molecular studies of an individual are presented here for the purpose of further characterizing… 
2000
2000
Tertiary trisomy due to a reciprocal translocation of chromosomes 5 and 21 in a four-generation family.
Tertiary trisomy, or double trisomy, is a rare occurrence. We present two individuals with a previously unreported tertiary… 
2000
2000
A novel gene, DSCR5, from the distal Down syndrome critical region on chromosome 21q22.2.
Based on a detailed sequence of the distal Down syndrome critical region (DSCR), we predicted and molecularly cloned a novel gene… 
1998
1998
Mapping of a novel human carbonyl reductase, CBR3, and ribosomal pseudogenes to human chromosome 21q22.2.
To find the genes contributing to Down syndrome, we constructed a 4-Mb sequence-ready map spanning chromosome 21q22.2 with… 
1996
1996
An integrated map with cosmid/PAC contigs of a 4-Mb Down syndrome critical region.
The major phenotypic features of Down syndrome have been correlated with partial trisomies of chromosome 21, allowing us to… 
1989
1989
Translocation (3;21) in Philadelphia positive chronic myeloid leukemia: high resolution chromosomal analysis and immunological study on five new cases.
Translocation t(3;21)(q26;q22) is a rare but nonrandom event occurring in Philadelphia positive chronic myeloid leukemia. We… 
1989
1989
Refined sublocalization of the human gene encoding the beta subunit of the S100 protein (S100B) and confirmation of a subtle t(9;21) translocation using in situ hybridization.
The gene which encodes the beta subunit of the S100 protein was mapped to 21q22.2----q22.3 by in situ hybridization. Concurrently… 
1982
1982
[Increased activity of adenine phosphoribosyl transferase in a child trisomic for 16q22.2 to 16qter due to malsegregation of a t(16;21) (q22.2;q22;2)pat (author's transl)].
Two cousins with trisomy for the distal third of 16q due to a familial translocation, t(16;21)(q22.2;q22-2), are reported. The… 
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