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12p12.3

A chromosome band present on 12p
National Institutes of Health

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2011
2011
Purpose: To study the inheritance and characteristics of familial Meniere disease in Finland and genetic linkage to the… Expand
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2010
2010
Meniere's disease (MD) is a disorder of the inner ear characterized by episodes of vertigo, tinnitus and fluctuating… Expand
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2006
2006
Meniere's disease (MD) is characterized by spontaneous attacks of vertigo, fluctuating sensorineural hearing loss, tinnitus, and… Expand
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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
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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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1999
1999
FISH analyses and loss of heterozygosity studies have delineated a commonly deleted region in hematological malignancies flanked… 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
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1997
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
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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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