A PAX3 polymorphism (T315K) in a family exhibiting Waardenburg Syndrome Type 2 (WS2)

By Wang C.   Kim E.   Attaie A.   Smith T.N.   Wilcox E.R.   Lalwani A.K.  

Molecular and Cellular Probes, Vol. 12, Iss. 1, 1998-02 ,pp. : 55-57

Academic Press

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Two different PAX3 gene mutations causing Waardenburg syndrome type I

By Wildhardt G.   Winterpacht A.   Hilbert K.   Menger H.   Zabel B.  

Molecular and Cellular Probes, Vol. 10, Iss. 3, 1996-03 ,pp. : 229-231

Academic Press

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A splice-site mutation affecting the paired box of PAX3 in a three generation family with Waardenburg syndrome type I (WS1)

By Attaie A.   Kim E.   Wilcox E.R.   Lalwani A.K.  

Molecular and Cellular Probes, Vol. 11, Iss. 3, 1997-03 ,pp. : 233-236

Academic Press

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Human pigmentation genes: identification, structure and consequences of polymorphic variation

By Sturm R.A.   Teasdale R.D.   Box N.F.  

Gene, Vol. 277, Iss. 1, 2001-10 ,pp. : 49-62

Elsevier

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Identification of Target Genes Regulated by PAX3 and PAX3–FKHR in Embryogenesis and Alveolar Rhabdomyosarcoma

By Barber T.D.   Barber M.C.   Tomescu O.   Barr F.G.   Ruben S.   Friedman T.B.  

Genomics, Vol. 79, Iss. 3, 2002-03 ,pp. : 278-284

Academic Press

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