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

Access to resources Recommend Favorite

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

Access to resources Recommend Favorite

A novel mutation in the MITF gene causes Waardenburg Syndrome Type 2

By Lautenschlager N.T.   Milunsky A.   DeStefano A.   Farrer L.   Baldwin C.T.  

Genetic Analysis: Biomolecular Engineering, Vol. 13, Iss. 2, 1996-07 ,pp. : 43-44

Elsevier

Access to resources Recommend Favorite

Effects of Pax3 Modifier Genes on Craniofacial Morphology, Pigmentation, and Viability: A Murine Model of Waardenburg Syndrome Variation

By Asher Jr J.H.   Harrison R.W.   Morell R.   Carey M.L.   Friedman T.B.  

Genomics, Vol. 34, Iss. 3, 1996-05 ,pp. : 285-298

Academic Press

Access to resources Recommend Favorite

Role of Pax Genes in Eye Evolution - A Cnidarian PaxB Gene Uniting Pax2 and Pax6 Functions

By Kozmik Z.   Daube M.   Frei E.   Norman B.   Kos L.   Dishaw L.J.   Noll M.   Piatigorsky J.  

Developmental Cell, Vol. 5, Iss. 5, 2003-11 ,pp. : 773-785

Elsevier

Access to resources Recommend Favorite