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21q22.3

A chromosome band present on 21q
National Institutes of Health

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Highly Cited
2008
Highly Cited
2008
Fundamental processes influencing human growth can be revealed by studying extreme short stature. Using genetic linkage analysis… Expand
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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… Expand
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Highly Cited
2003
Highly Cited
2003
The cystathionine beta synthase (CBS) gene is localized on chromosome 21 (21q22.3). This enzyme is one of three enzymes able to… Expand
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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… Expand
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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… Expand
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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… Expand
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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… Expand
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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… Expand
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Highly Cited
1994
Highly Cited
1994
Autoimmune polyglandular disease type I (APECED) is an autosomal recessive autoimmune disease characterized by a variable… Expand
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Highly Cited
1994
Highly Cited
1994
Holoprosencephaly (HPE) is a common malformation of the developing forebrain and midface characterized by incomplete penetrance… Expand
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