Welp CL - Search Results

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GJB2: the spectrum of deafness-causing allele variants and their phenotype.

Azaiez H, Chamberlin GP, Fischer SM, Welp CL, Prasad SD, Taggart RT, del Castillo I, Van Camp G, Smith RJ. Azaiez H, et al. Among authors: welp cl. Hum Mutat. 2004 Oct;24(4):305-11. doi: 10.1002/humu.20084. Hum Mutat. 2004. PMID: 15365987 Free PMC article.

Transient early embryonic expression of Nkx2-5 mutations linked to congenital heart defects in human causes heart defects in Xenopus laevis.

Bartlett HL, Sutherland L, Kolker SJ, Welp C, Tajchman U, Desmarais V, Weeks DL. Bartlett HL, et al. Dev Dyn. 2007 Sep;236(9):2475-84. doi: 10.1002/dvdy.21244. Dev Dyn. 2007. PMID: 17685485 Free PMC article.

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