21q22.3

A chromosome band present on 21q
National Institutes of Health

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Highly Cited
2008
Highly Cited
2008
OBJECTIVE The Type 1 Diabetes Genetics Consortium (T1DGC) has assembled and genotyped a large collection of multiplex families… (More)
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Highly Cited
2008
Highly Cited
2008
Large brain size is one of the defining characteristics of modern humans. Seckel syndrome (MIM 210600), a disorder of markedly… (More)
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Highly Cited
2006
Highly Cited
2006
Prostate cancer is a common and clinically heterogeneous disease with marked variability in progression. The recent… (More)
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Highly Cited
2000
Highly Cited
2000
We have isolated the DNMT3L gene that is related to the cytosine-5-methyltransferase 3 (DNMT3) family. The gene is located on… (More)
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Highly Cited
1998
Highly Cited
1998
Congenital cataracts are a common major abnormality of the eye that frequently cause blindness in infants. At least a third of… (More)
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Highly Cited
1997
Highly Cited
1997
Autoimmune polyglandular syndrome type I (APS 1, also called APECED) is an autosomal-recessive disorder that maps to human… (More)
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Highly Cited
1997
Highly Cited
1997
To contribute to the development of the transcription map of human chromosome 21 (HC21), we have used exon trapping from pools of… (More)
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1996
1996
Deafness is a heterogeneous trait affecting approximately 1/1,000 newborns. Genetic linkage studies have already implicated more… (More)
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Highly Cited
1996
Highly Cited
1996
Progressive myoclonus epilepsy of the Unverricht-Lundborg type (EPM1) is an autosomal recessive inherited form of epilepsy… (More)
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Highly Cited
1994
Highly Cited
1994
In a preliminary genome scan of 47 bipolar disorder families, we detected in one family a lod score of 3.41 at the PFKL locus on… (More)
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