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Results: 1-6 |
Results: 6

Authors: Wessagowit, V Ashton, GHS Mohammedi, R Salas-Alanis, JC Denyer, JE Mellerio, JE Eady, RAJ McGrath, JA
Citation: V. Wessagowit et al., Three cases of de novo dominant dystrophic epidermolysis bullosa associated with the mutation G2043R in COL7A1, CLIN EXP D, 26(1), 2001, pp. 97-99

Authors: Salas-Alanis, JC Amaya-Guerra, M McGrath, JA
Citation: Jc. Salas-alanis et al., The molecular basis of dystrophic epidermolysis bullosa in Mexico, INT J DERM, 39(6), 2000, pp. 436-442

Authors: Salas-Alanis, JC Mellerio, JE Ashton, GHS McGrath, JA
Citation: Jc. Salas-alanis et al., Frequency of the CCR5 gene 32-basepair deletion in Hispanic Mexicans, CLIN EXP D, 24(2), 1999, pp. 127-129

Authors: McGrath, JA Ashton, GHS Mellerio, JE Salas-Alanis, JC Swensson, O McMillan, JR Eady, RAJ
Citation: Ja. Mcgrath et al., Moderation of phenotypic severity in dystrophic and junctional forms of epidermolysis bullosa through in-frame skipping of exons containing non-senseor frameshift mutations, J INVES DER, 113(3), 1999, pp. 314-321

Authors: Mellerio, JE Ashton, GHS Mohammedi, R Lyon, CC Kirby, B Harman, KE Salas-Alanis, JC Atherton, DJ Harrison, PV Griffiths, WAD Black, MM Eady, RAJ McGrath, JA
Citation: Je. Mellerio et al., Allelic heterogeneity of dominant and recessive COL7A1 mutations underlying epidermolysis bullosa pruriginosa, J INVES DER, 112(6), 1999, pp. 984-987

Authors: Cserhalmi-Friedman, PB McGrath, JA Mellerio, JE Romero, R Salas-Alanis, JC Paller, AS Dietz, HC Christiano, AM
Citation: Pb. Cserhalmi-friedman et al., Restoration of open reading frame resulting from skipping of an exon with an internal deletion in the COL7A1 gene, LAB INV, 78(12), 1998, pp. 1483-1492
Risultati: 1-6 |