Isolation of the defective gene in X linked agammaglobulinaemia.

Por Vetrie, D
Publicado em 1993

Pelizaeus-Merzbacher disease: identification of Xq22 proteolipid-protein duplications and characterization of breakpoints by interphase FISH.

Por Woodward, K, Kendall, E, Vetrie, D, Malcolm, S
Publicado em 1998

X inactivation patterns in females with Alport's syndrome: a means of selecting against a deleterious gene?

Por Vetrie, D, Flinter, F, Bobrow, M, Harris, A
Publicado em 1992

X inactivation as a mechanism of selection against lethal alleles: further investigation of incontinentia pigmenti and X linked lymphoproliferative disease.

Por Harris, A, Collins, J, Vetrie, D, Cole, C, Bobrow, M
Publicado em 1992

Somatic mosaicism associated with a mild Alport syndrome phenotype

Por PLANT, K., BOYE, E., GREEN, P., VETRIE, D., FLINTER, F.
Publicado em 2000

Structural instability of human tandemly repeated DNA sequences cloned in yeast artificial chromosome vectors.

Por Neil, D L, Villasante, A, Fisher, R B, Vetrie, D, Cox, B, Tyler-Smith, C
Publicado em 1990

Position effect on PLP1 may cause a subset of Pelizaeus-Merzbacher disease symptoms

Por Muncke, N, Wogatzky, B, Breuning, M, Sistermans, E, Endris, V, Ross, M, Vetrie, D, Catsman-Berrevoet..., C, Rappold, G
Publicado em 2004

Structural basis for chromosome X-linked agammaglobulinemia: a tyrosine kinase disease.

Por Vihinen, M, Vetrie, D, Maniar, H S, Ochs, H D, Zhu, Q, Vorechovský, I, Webster, A D, Notarangelo, L D, Nilsson, L, Sowadski, J M
Publicado em 1994

Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array‐CGH

Por Mantripragada, K K, Thuresson, A‐C, Piotrowski, A, de Ståhl, T Díaz, Menzel, U, Grigelionis, G, Ferner, R E, Griffiths, S, Bolund, L, Mautner, V, Nordling, M, Legius, E, Vetrie, D, Dahl, N, Messiaen, L, Upadhyaya, M, Bruder, C E G, Dumanski, J P
Publicado em 2006