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Chromosome 21 Short Arm

Known as: 21p, Chromosome 21 Proximal Arm 
Proximal (short) arm of chromosome 21
National Institutes of Health

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3 relations
ChromosomesChromosomes, Human, Pair 21MIR155 wt Allele

Papers overview

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2014
2014
Prenatal diagnosis of isochromosome 21p and isochromosome 21q in a fetus with Down syndrome.
The aim of this study was to present the first case with Down syndrome in conjunction with de novo isochromosomes of both short… 
2009
2009
[Detection of the genetic abnormalities in patients with mental retardation using multiplex ligation-dependent probe amplification assay].
OBJECTIVE To investigate the relationship between subtelomeric rearrangements and idiopathic mental retardation (MR). METHODS… 
2009
2009
SALSA MLPA KIT P036-E1 HUMAN TELOMERE-3
  • 2009
  • Corpus ID: 49579920
MENTAL RETARDATION is caused by aberrant copy numbers of subtelomeric regions in 3-8 % of all cases. This P036-E1 human telomere… 
2006
2006
Mesotheliomas Region of Chromosomal Loss in Human Malignant Homozygous Deletions within 9 p 21p 22 Identify a Small Critical
Previous DNA analyses have demonstrated that 9pl3-p22 is a frequent site of chromosomal loss in leukemia, glioma, melanoma, and… 
2002
2002
Two new cases of the Christchurch (Ch1) chromosome 21: evidence for clinical consequences of de novo deletion 21P-.
We performed an investigation of two unrelated cases with extremal variants of chromosome 21 without visible materials of the… 
2002
2002
Advances in Brief Functional Evidence for a Metastasis Suppressor Gene for Rat Prostate Cancer within a 60-Kilobase Region on Human Chromosome 8 p 21p 121
We recently demonstrated that the human chromosome 8p21-p12 region encodes a metastasis suppressor gene for rat prostate cancer… 
2000
2000
A Role for Cytosolic Hsp 70 in Yeast [ PSI 1 ] Prion Propagation and [ PSI 1 ] as a Cellular Stress
[PSI] is a prion (infectious protein) of Sup35p, a subunit of the Saccharomyces cerevisiae translation termination factor. We… 
1994
1994
Assessment of Yqh translocations.
Two initially presumed Yqh translocations, one to Xp and another to 21p, were assessed by conventional banding procedures, 5… 
1993
1993
Cytogenetic, FISH and DNA studies in 11 individuals from a family with two siblings with dup(21q) Down syndrome
A Spanish family has previously been described with two siblings with dup(21q) Down syndrome. The father has a normal karyotype… 
Review
1976
Review
1976
De novo appearance of a translocation t(5p; 2Iq), and its transmission in both balanced and unbalanced forms to the next generation.
A family is described in which a reciprocal translocation involving 5p and 21q appeared de novo in the chromosome complement of a… 
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