Screening for Down's syndrome in the North East Thames region.

Por Murday, V, Slack, J
Publicado em 1985

Cancer and the Peutz-Jeghers syndrome.

Por Spigelman, A D, Murday, V, Phillips, R K
Publicado em 1989

Biliary hypoplasia in Williams syndrome

Por O'Reilly, K, Ahmed, S F, Murday, V, McGrogan, P
Publicado em 2006

Screening and genetic counselling for relatives of patients with colorectal cancer in a family cancer clinic.

Por Houlston, R S, Murday, V, Harocopos, C, Williams, C B, Slack, J
Publicado em 1990

The impact of genetic counselling on risk perception and mental health in women with a family history of breast cancer

Por Watson, M, Lloyd, S, Davidson, J, Meyer, L, Eeles, R, Ebbs, S, Murday, V
Publicado em 1999

Muir-Torre syndrome: a variant of the cancer family syndrome.

Por Hall, N R, Williams, M A, Murday, V A, Newton, J A, Bishop, D T
Publicado em 1994

Confirmation of CHD7 as a cause of CHARGE association identified by mapping a balanced chromosome translocation in affected monozygotic twins

Por Johnson, D, Morrison, N, Grant, L, Turner, T, Fantes, J, Connor, J M, Murday, V
Publicado em 2006

A survey of phenotypic features in juvenile polyposis.

Por Desai, D C, Murday, V, Phillips, R K, Neale, K F, Milla, P, Hodgson, S V
Publicado em 1998

PTEN mutations are uncommon in Proteus syndrome

Por Barker, K, Martinez, A, Wang, R, Bevan, S, Murday, V, Shipley, J, Houlston, R, Harper, J
Publicado em 2001

Feasibility of family based screening for colorectal neoplasia: experience in one general surgical practice.

Por Stephenson, B M, Murday, V A, Finan, P J, Quirke, P, Dixon, M F, Bishop, D T
Publicado em 1993

Family history of breast cancer: what do women understand and recall about their genetic risk?

Por Watson, M, Duvivier, V, Wade Walsh, M, Ashley, S, Davidson, J, Papaikonomou, M, Murday, V, Sacks, N, Eeles, R
Publicado em 1998

Cowden syndrome and Lhermitte-Duclos disease in a family: a single genetic syndrome with pleiotropy?

Por Eng, C, Murday, V, Seal, S, Mohammed, S, Hodgson, S V, Chaudary, M A, Fentiman, I S, Ponder, B A, Eeles, R A
Publicado em 1994

Balancing autonomy and responsibility: the ethics of generating and disclosing genetic information

Por Hallowell, N, Foster, C, Eeles, R, Ardern-Jones, A, Murday, V, Watson, M, Clarke, A, Hallowell, N, Watson, M
Publicado em 2003

Familial dilated cardiomyopathy in the United Kingdom.

Por Keeling, P. J., Gang, Y., Smith, G., Seo, H., Bent, S. E., Murday, V., Caforio, A. L., McKenna, W. J.
Publicado em 1995

CpG island clones from a deletion encompassing the gene for adenomatous polyposis coli.

Por Varesco, L, Thomas, H J, Cottrell, S, Murday, V, Fennell, S J, Williams, S, Searle, S, Sheer, D, Bodmer, W F, Frischauf, A M
Publicado em 1989

Reduction of the genetic interval for lymphoedema-distichiasis to below 2 Mb

Por BELL, R, BRICE, G, CHILD, A, MURDAY, V, MANSOUR, S, SANDY, C, COLLIN, J, MORTIMER, P, CALLEN, D, BURNAND, K, JEFFERY, S
Publicado em 2000

Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24

Por Brice, G, Mansour, S, Bell, R, Collin, J, Child, A, Brady, A, Sarfarazi, M, Burnand, K, Jeffery, S, Mortimer, P, Murday, V
Publicado em 2002

Linkage analysis of early-onset breast and ovarian cancer families, with markers on the long arm of chromosome 17.

Por Spurr, N K, Kelsell, D P, Black, D M, Murday, V A, Turner, G, Crockford, G P, Solomon, E, Cartwright, R A, Bishop, D T
Publicado em 1993

A randomised comparison of UK genetic risk counselling services for familial cancer: psychosocial outcomes

Por Hopwood, P, Wonderling, D, Watson, M, Cull, A, Douglas, F, Cole, T, Eccles, D, Gray, J, Murday, V, Steel, M, Burn, J, McPherson, K
Publicado em 2004

Germline PTEN mutations in Cowden syndrome-like families.

Por Marsh, D J, Dahia, P L, Caron, S, Kum, J B, Frayling, I M, Tomlinson, I P, Hughes, K S, Eeles, R A, Hodgson, S V, Murday, V A, Houlston, R, Eng, C
Publicado em 1998