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WDR11 gene

Known as: HH14, WDR11, BRWD2, FORMERLY 
 
National Institutes of Health

Papers overview

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Review
2017
Review
2017
Context: Pituitary stalk interruption syndrome (PSIS, ORPHA95496) is a congenital defect of the pituitary gland characterized by… Expand
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Highly Cited
2012
Highly Cited
2012
OBJECTIVE To investigate the association of anti-hydroxymethylglutaryl-coenzyme A reductase (anti-HMGCR) myopathy with HLA class… Expand
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Highly Cited
2010
Highly Cited
2010
By defining the chromosomal breakpoint of a balanced t(10;12) translocation from a subject with Kallmann syndrome and scanning… Expand
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2007
2007
Primary sclerosing cholangitis (PSC) is associated with the human leukocyte antigen (HLA)-DRB1*0301-DQA1*0501-DQB1*0201 (DR3) and… Expand
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2003
2003
Oncogenes and tumor suppressor genes are clustered around recombination hot spots or fragile sites in the genome, because double… Expand
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2001
2001
OBJECTIVE To determine the frequency of shared epitopes in our population of patients with rheumatoid arthritis (RA) and to… Expand
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2001
2001
Allelic deletions of 10q25–26 and 19q13.3–13.4 are the most common genetic alterations in glial tumors. We have identified a… Expand
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2000
2000
OBJECTIVE To test for linkage between the HLA region and juvenile rheumatoid arthritis (JRA), with stratification by onset and… Expand
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Highly Cited
1996
Highly Cited
1996
Segmentation of the neural tube has been clearly shown in the forebrain and caudal hindbrain but has never been demonstrated… Expand
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1994
1994
Graves' disease (GD) is an autoimmune thyroid disease and is associated with human leukocyte antigen (HLA)-DR3 and -DQA1*0501 in… Expand
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