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Temtamy Preaxial Brachydactyly Syndrome Is Caused by Loss-of-Function Mutations in Chondroitin Synthase 1, a Potential Target of BMP SignalingYUN LI; LAUE, Kathrin; QUARRELL, Oliver W et al.American journal of human genetics. 2010, Vol 87, Num 6, pp 757-767, issn 0002-9297, 11 p.Article

Mutations in TPRN Cause a Progressive Form of Autosomal-Recessive Nonsyndromic Hearing LossYUN LI; POHL, Esther; VELTMAN, Joris A et al.American journal of human genetics. 2010, Vol 86, Num 3, pp 479-484, issn 0002-9297, 6 p.Article

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