Rapid RFLP screening using DNA from complete hydatidiform moles.

od Litt, M, Buder, A, Surti, U
Wydane 1989

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

od Surti, U, Hoffner, L, Chakravarti, A, Ferrell, R E
Wydane 1990

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

od Vejerslev, L O, Fisher, R A, Surti, U, Wake, N
Wydane 1987

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

od Walter, M A, Surti, U, Hofker, M H, Cox, D W
Wydane 1990

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

od Zaragoza, M V, Surti, U, Redline, R W, Millie, E, Chakravarti, A, Hassold, T J
Wydane 2000

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

od Pegoraro, E, Whitaker, J, Mowery-Rushton, P, Surti, U, Lanasa, M, Hoffman, E P
Wydane 1997

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

od Wolff, D. J., Brown, C. J., Schwartz, S., Duncan, A. M., Surti, U., Willard, H. F.
Wydane 1994

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

od Deka, R, Chakravarti, A, Surti, U, Hauselman, E, Reefer, J, Majumder, P P, Ferrell, R E
Wydane 1990

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

od Glenn, C. C., Saitoh, S., Jong, M. T., Filbrandt, M. M., Surti, U., Driscoll, D. J., Nicholls, R. D.
Wydane 1996

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

od Dufresne, SD, Felgar, RE, Sargent, RL, Surti, U, Gollin, SM, McPhail, ED, Cook, JR, Swerdlow, SH
Wydane 2009

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

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

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

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

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

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

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

od 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
Wydane 2006

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

od 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.
Wydane w Clin Genet (2015)