PHF6 wt Allele

Known as: CENP-31, BORJ, MGC14797 
Human PHF6 wild-type allele is located in the vicinity of Xq26.3 and is approximately 56 kb in length. This allele, which encodes PHD finger protein… (More)
National Institutes of Health

Topic mentions per year

Topic mentions per year

1984-2006
0119842006

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2006
2006
BACKGROUND Börjeson-Forssman-Lehmann syndrome (BFLS; MIM 301900) is an infrequently described X linked disorder caused by… (More)
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2005
2005
1962 berichteten Börjeson, Forssman und Lehmann erstmals über das seltene Krankheitsbild des BFLS. Diese Krankheit wird X… (More)
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2004
2004
The Börjeson–Forsmann–Lehmann syndrome (BFLS, (MIM 301900)) was first described by one of us in 1962 in a family with severe X… (More)
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1996
1996
A detailed map of genetic markers was constructed around the gene for the X-linked mental retardation syndrome of Börjeson… (More)
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1984
1984
We have studied five males with Börjeson-Forssman-Lehmann syndrome (BFLS) from two unrelated families. They had a characteristic… (More)
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