RICHARD GIBBS to Bardet-Biedl Syndrome
This is a "connection" page, showing publications RICHARD GIBBS has written about Bardet-Biedl Syndrome.
Connection Strength
0.132
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Recurrent CNVs and SNVs at the NPHP1 locus contribute pathogenic alleles to Bardet-Biedl syndrome. Am J Hum Genet. 2014 May 01; 94(5):745-54.
Score: 0.112
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A common allele in RPGRIP1L is a modifier of retinal degeneration in ciliopathies. Nat Genet. 2009 Jun; 41(6):739-45.
Score: 0.020