au.\*:("D'SOUZA, V. N")
Results 1 to 5 of 5
Selection :
Cloning and characterization of alternatively spliced isoforms of Dp71AUSTIN, R. C; HOWARD, P. L; D'SOUZA, V. N et al.Human molecular genetics (Print). 1995, Vol 4, Num 9, pp 1475-1483, issn 0964-6906Article
A splice-junction mutation in the region of COL5A1 that codes for the carboxyl propeptide of proα1(V) chains results in the gravis form of the Ehlers-Danlos syndrome (type I)WENSTRUP, R. J; LANGLAND, G. T; WILLING, M. C et al.Human molecular genetics (Print). 1996, Vol 5, Num 11, pp 1733-1736, issn 0964-6906Article
A novel dystrophin isoform is required for normal retinal electrophysiologyD'SOUZA, V. N; NGUYEN THI MAN; MORRIS, G. E et al.Human molecular genetics (Print). 1995, Vol 4, Num 5, pp 837-842, issn 0964-6906Article
Genomic organization of exons 22 to 25 of the dystrophin geneBEBCHUK, K. G; BULMAN, D. E; D'SOUZA, V. N et al.Human molecular genetics (Print). 1993, Vol 2, Num 5, pp 594-595, issn 0964-6906Article
IFNG +874 T>A single nucleotide polymorphism is associated with leprosy among BraziliansCARDOSO, C. C; PEREIRA, A. C; PACHECO, A. G et al.Human genetics. 2010, Vol 128, Num 5, pp 481-490, issn 0340-6717, 10 p.Article