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6q24

A chromosome band present on 6q
National Institutes of Health

Papers overview

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Highly Cited
2013
Highly Cited
2013
Aims/hypothesis6q24 transient neonatal diabetes mellitus (TNDM) is a rare form of diabetes presenting in the neonatal period that… Expand
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Highly Cited
2010
Highly Cited
2010
There is increasing evidence that the microcirculation plays an important role in the pathogenesis of cardiovascular diseases… Expand
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Highly Cited
2008
Highly Cited
2008
PURPOSE Early/initiating oncogenic mutations have been identified for many cancers, but such mutations remain unidentified in… Expand
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Highly Cited
2008
Highly Cited
2008
Background/objective:  Mutations in KCNJ11, ABCC8, or INS are the cause of permanent neonatal diabetes mellitus in about 50% of… Expand
Highly Cited
2005
Highly Cited
2005
Familial hemophagocytic lymphohistiocytosis (FHL) is a rare autosomal recessive disorder characterized by hyperactive phagocytes… Expand
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Highly Cited
2005
Highly Cited
2005
Identification of genetic variants that contribute to risk of hypertension is challenging. As a complement to linkage and… Expand
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Highly Cited
2003
Highly Cited
2003
LOT1 is a zinc-finger nuclear transcription factor, which possesses anti-proliferative effects and is frequently silenced in… Expand
Highly Cited
2000
Highly Cited
2000
Transient neonatal diabetes (TND) is a rare type of diabetes that presents soon after birth, resolves by 18 months, and… Expand
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Highly Cited
1998
Highly Cited
1998
Lafora's disease (LD; OMIM 254780) is an autosomal recessive form of progressive myoclonus epilepsy characterized by seizures and… Expand
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Highly Cited
1994
Highly Cited
1994
A human mu opiate receptor cDNA has been identified from a cerebral cortical cDNA library using sequences from the rat mu opiate… Expand
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