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12p12.3

A chromosome band present on 12p
National Institutes of Health

Papers overview

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2014
2014
Colorectal cancer (CRC) is one of the most common cancer worldwide. However, a large number of genetic risk factors involved in… Expand
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Highly Cited
2006
Highly Cited
2006
Meniere's disease (MD) is characterized by spontaneous attacks of vertigo, fluctuating sensorineural hearing loss, tinnitus, and… Expand
Highly Cited
2001
Highly Cited
2001
Type A receptors of gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter, contain alpha, beta, delta, gamma, and rho… Expand
Highly Cited
1999
Highly Cited
1999
Keutel syndrome (KS, MIM 245150) is an autosomal recessive disorder characterized by abnormal cartilage calcification, peripheral… Expand
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Review
1999
Review
1999
Cytogenetic deletions on the short arm of chromosome 12 are common, recurring alterations found in a wide range of hematological… Expand
1999
1999
FISH analyses and loss of heterozygosity studies have delineated a commonly deleted region in hematological malignancies flanked… Expand
Highly Cited
1997
Highly Cited
1997
Identification of the key genetic alterations leading to ovarian cancer is in its infancy. Polymerase chain reaction (PCR)-based… Expand
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1997
1997
Cytogenetic deletions of the short arm of chromosome 12 are common recurring alterations found in a wide range of haematological… Expand
Highly Cited
1996
Highly Cited
1996
Together with the 31-kDa microfibril-associated glycoprotein (MAGP), four polypeptides designated MP340 (340 kDa), MP78 (78 kDa… Expand
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1981
1981
A complex de novo translocation was found in leukocytes and fibroblasts from a boy with mental retardation and minor… Expand