Rapid RFLP screening using DNA from complete hydatidiform moles.

Por Litt, M, Buder, A, Surti, U
Publicado em 1989

Genetics and biology of human ovarian teratomas. I. Cytogenetic analysis and mechanism of origin.

Por Surti, U, Hoffner, L, Chakravarti, A, Ferrell, R E
Publicado em 1990

Hydatidiform mole: parental chromosome aberrations in partial and complete moles.

Por Vejerslev, L O, Fisher, R A, Surti, U, Wake, N
Publicado em 1987

The physical organization of the human immunoglobulin heavy chain gene complex.

Por Walter, M A, Surti, U, Hofker, M H, Cox, D W
Publicado em 1990

Parental origin and phenotype of triploidy in spontaneous abortions: predominance of diandry and association with the partial hydatidiform mole.

Por Zaragoza, M V, Surti, U, Redline, R W, Millie, E, Chakravarti, A, Hassold, T J
Publicado em 2000

Familial skewed X inactivation: a molecular trait associated with high spontaneous-abortion rate maps to Xq28.

Por Pegoraro, E, Whitaker, J, Mowery-Rushton, P, Surti, U, Lanasa, M, Hoffman, E P
Publicado em 1997

Small marker X chromosomes lack the X inactivation center: implications for karyotype/phenotype correlations.

Por Wolff, D. J., Brown, C. J., Schwartz, S., Duncan, A. M., Surti, U., Willard, H. F.
Publicado em 1994

Genetics and biology of human ovarian teratomas. II. Molecular analysis of origin of nondisjunction and gene-centromere mapping of chromosome I markers.

Por Deka, R, Chakravarti, A, Surti, U, Hauselman, E, Reefer, J, Majumder, P P, Ferrell, R E
Publicado em 1990

Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene.

Por Glenn, C. C., Saitoh, S., Jong, M. T., Filbrandt, M. M., Surti, U., Driscoll, D. J., Nicholls, R. D.
Publicado em 1996

Defining the Borders of Splenic Marginal Zone Lymphoma: A Multiparameter Study

Por Dufresne, SD, Felgar, RE, Sargent, RL, Surti, U, Gollin, SM, McPhail, ED, Cook, JR, Swerdlow, SH
Publicado em 2009

Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients.

Por Christian, S L, Robinson, W P, Huang, B, Mutirangura, A, Line, M R, Nakao, M, Surti, U, Chakravarti, A, Ledbetter, D H
Publicado em 1995

Identification of an unbalanced cryptic translocation t(9;17)(q34.3;p13.3) in a child with dysmorphic features

Por Estop, A M, Mowery-Rushton, P A, Cieply, K M, Kochmar, S J, Sherer, C R, Clemens, M, Surti, U, McPherson, E
Publicado em 1995

Content and organization of the human Ig VH locus: definition of three new VH families and linkage to the Ig CH locus.

Por Berman, J E, Mellis, S J, Pollock, R, Smith, C L, Suh, H, Heinke, B, Kowal, C, Surti, U, Chess, L, Cantor, C R
Publicado em 1988

Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative study

Por Graf, M D, Christ, L, Mascarello, J T, Mowrey, P, Pettenati, M, Stetten, G, Storto, P, Surti, U, Van Dyke, D L, Vance, G H, Wolff, D, Schwartz, S
Publicado em 2006

High-resolution microarray analysis unravels complex Xq28 aberrations in patients and carriers affected by X-linked blue cone monochromacy

Por Yatsenko, S.A., Bakos, H.A., Vitullo, K., Kedrov, M., Kishore, A., Jennings, B.J., Surti, U., Wood-Trageser, M.A., Cercone, S., Yatsenko, A.N., Rajkovic, A., Iannaccone, A.
Publicado no Clin Genet (2015)