WEIMIN BI to Limb Deformities, Congenital
This is a "connection" page, showing publications WEIMIN BI has written about Limb Deformities, Congenital.
Connection Strength
0.139
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A male newborn with VACTERL association and Fanconi anemia with a FANCB deletion detected by array comparative genomic hybridization (aCGH). Am J Med Genet A. 2011 Dec; 155A(12):3071-4.
Score: 0.085
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Inactivation of Rai1 in mice recapitulates phenotypes observed in chromosome engineered mouse models for Smith-Magenis syndrome. Hum Mol Genet. 2005 Apr 15; 14(8):983-95.
Score: 0.054