Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24).

Por Haddad, B R, Lin, A E, Wyandt, H, Milunsky, A
Publicado em 1996

Alterations in Cell Motility, Proliferation, and Metabolism in Novel Models of Acquired Temozolomide Resistant Glioblastoma

Por Tiek, D. M., Rone, J. D., Graham, G. T., Pannkuk, E. L., Haddad, B. R., Riggins, R. B.
Publicado no Sci Rep (2018)

Loss of heterozygosity of the BRCA1 and FHIT genes in patients with sporadic breast cancer from Southern Brazil

Por Santos, S C L, Cavalli, L R, Cavalli, I J, Lima, R S, Haddad, B R, Ribeiro, E M S F
Publicado em 2004

Frequent Loss of the BLID Gene in Early-Onset Breast Cancer

Por Cavalli, L.R., Noone, A.-M., Makambi, K.H., Rone, J.D., Kasid, U.N., Haddad, B.R.
Publicado em 2011

Assignment of the BLID gene to 11q24.1 by fluorescence in situ hybridization

Por Cavalli, L.R., Santos, S.C.L., Broustas, C.G., Rone, J.D., Kasid, U.N., Haddad, B.R.
Publicado no Cancer Genet Cytogenet (2008)

Evaluation of paediatric osteosarcomas by classic cytogenetic and CGH analyses

Por Batanian, J R, Cavalli, L R, Aldosari, N M, Ma, E, Sotelo-Avila, C, Ramos, M B, Rone, J D, Thorpe, C M, Haddad, B R
Publicado em 2002

Multicolour FISH and quantitative PCR can detect submicroscopic deletions in holoprosencephaly patients with a normal karyotype

Por Bendavid, C, Haddad, B R, Griffin, A, Huizing, M, Dubourg, C, Gicquel, I, Cavalli, L R, Pasquier, L, Shanske, A L, Long, R, Ouspenskaia, M, Odent, S, Lacbawan, F, David, V, Muenke, M
Publicado em 2006

TGIF Mutations in Human Holoprosencephaly: Correlation between Genotype and Phenotype

Por Keaton, A.A., Solomon, B.D., Kauvar, E.F., El-Jaick, K.B., Gropman, A.L., Zafer, Y., Meck, J.M., Bale, S.J., Grange, D.K., Haddad, B.R., Gowans, G.C., Clegg, N.J, Delgado, M.R., Hahn, J.S., Pineda-Alvarez, D.E., Lacbawan, F., Vélez, J.I., Roessler, E., Muenke, M.
Publicado em 2011