Congenital Constrictions on Leg and Arm

Por Bulman, M. W.
Publicado em 1930

Congenital Scoliosis

Por Bulman, M. W.
Publicado em 1930

Sensitivity of BRCA1/2 mutation testing in 466 breast/ovarian cancer families

Por Evans, D, Bulman, M, Young, K, Gokhale, D, Lalloo, F
Publicado em 2003

Haplotype and cancer risk analysis of two common mutations, BRCA1 4184del4 and BRCA2 2157delG, in high risk northwest England breast/ovarian families

Por Evans, D, Neuhausen, S, Bulman, M, Young, K, Gokhale, D, Lalloo, F
Publicado em 2004

A gene for autosomal recessive spondylocostal dysostosis maps to 19q13.1-q13.3.

Por Turnpenny, P D, Bulman, M P, Frayling, T M, Abu-Nasra, T K, Garrett, C, Hattersley, A T, Ellard, S
Publicado em 1999

A new scoring system for the chances of identifying a BRCA1/2 mutation outperforms existing models including BRCAPRO

Por Evans, D, Eccles, D, Rahman, N, Young, K, Bulman, M, Amir, E, Shenton, A, Howell, A, Lalloo, F
Publicado em 2004

Response to correspondence on “Phenocopies in BRCA1 and BRCA2 families: evidence for modifier genes and implications for screening”

Por Smith, A, Boyd, M C, Bulman, M, Shenton, A, Lalloo, F, Evans, D G R, Moran, A, Iddenden, R, Smith, L, Woodward, E R, Maher, E R
Publicado em 2007

Phenocopies in BRCA1 and BRCA2 families: evidence for modifier genes and implications for screening

Por Smith, A, Moran, A, Boyd, M C, Bulman, M, Shenton, A, Smith, L, Iddenden, R, Woodward, E R, Lalloo, F, Maher, E R, Evans, D G R
Publicado em 2007