19p13.3

A chromosome band present on 19p
National Institutes of Health

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Highly Cited
2009
Highly Cited
2009
We conducted a genome-wide association study among 2,323 individuals with sporadic amyotrophic lateral sclerosis (ALS) and 9,013… (More)
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Highly Cited
2002
Highly Cited
2002
Adolescent idiopathic scoliosis (AIS) is one of the most common orthopedic disorders, affecting up to 4% of schoolchildren… (More)
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Highly Cited
2001
Highly Cited
2001
Despite the growing awareness of intraductal papillary-mucinous neoplasms (IPMNs) of the pancreas among clinicians, the molecular… (More)
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Highly Cited
2000
Highly Cited
2000
Congenital neutropenia and cyclic neutropenia are disorders of neutrophil production predisposing patients to recurrent bacterial… (More)
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Highly Cited
1999
Highly Cited
1999
Cardiac pacemaking is produced by the slow diastolic depolarization phase of the action potential. The hyperpolarization… (More)
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Highly Cited
1999
Highly Cited
1999
Human cyclic haematopoiesis (cyclic neutropenia, MIM 162800) is an autosomal dominant disease in which blood-cell production from… (More)
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1999
1999
Germline mutations in the LKB1 (STK11) gene (chromosome sub-band 19p13.3) cause characteristic hamartomas and pigmentation to… (More)
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Review
1999
Review
1999
Peutz-Jeghers syndrome (PJS) is a classic, but not widely known hereditary trait. Its clinical hallmarks are intestinal… (More)
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Highly Cited
1998
Highly Cited
1998
Peutz-Jeghers (PJ) syndrome is an autosomal-dominant disorder characterized by melanocytic macules of the lips, multiple… (More)
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1998
1998
A locus for Peutz-Jeghers syndrome (PJS) was recently mapped to chromosome 19p13.3. Each of 12 families studied was compatible… (More)
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