THE CLINICOPATHOLOGIC PROFILE OF THE PARTIAL HYDATIDIFORM MOLESZULMAN AE; SURTI U.1982; OBSTET. GYNECOL. (N.Y., 1953); ISSN 0029-7844; USA; DA. 1982; VOL. 59; NO 5; PP. 597-602; BIBL. 22 REF.Article

THE SYNDROMES OF HYDATIDIFORM MOLE. I. MORPHOLOGIC EVOLUTION OF THE COMPLETE AND PARTIAL MOLESZULMAN AE; SURTI U.1978; AMER. J. OBSTETR. GYNECOL.; USA; DA. 1978; VOL. 132; NO 1; PP. 20-27; BIBL. 15 REF.Article

DISPERMIC ORIGIN AND CLINICAL OUTCOME OF THREE COMPLETE HYDATIDIFORM MOLES WITH 46, XY KARYOTYPESURTI U; SZULMAN AE; O'BRIEN S et al.1982; AM. J. OBSTET. GYNECOL.; ISSN 0002-9378; USA; DA. 1982; VOL. 144; NO 1; PP. 84-87; BIBL. 10 REF.Article

COMPLETE(CLASSIC) HYDATIDIFORM MOLE WITH 46,XY KARYOTYPE OF PATERNAL ORIGINSURTI U; SZULMAN AE; O'BRIEN S et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 51; NO 2; PP. 153-155; BIBL. 8 REF.Article

Subgroups of uterine leiomyomas based on cytogenetic analysisHU, J; SURTI, U.Human pathology. 1991, Vol 22, Num 10, pp 1009-1016, issn 0046-8177Article

Cytogenetics of trophoblasts from complete hydatidiform molesHABIBIAN, R; SURTI, U.Cancer genetics and cytogenetics. 1987, Vol 29, Num 2, pp 271-287, issn 0165-4608Article

Sister chromati exchange and chromosome breakage in complete hydatifiform molesBECKER, R. A; SURTI, U; WENGER, S. L et al.Cancer genetics and cytogenetics. 1992, Vol 62, Num 1, pp 53-57, issn 0165-4608Article

Cytogenetic analysis of a uterine lipoleiomyomaJIE HU; SURTI, U; TOBON, H et al.Cancer genetics and cytogenetics. 1992, Vol 62, Num 2, pp 200-202, issn 0165-4608Article

Delection of chromosome 13 in leiomyomas of the uterusMELONI, A. M; SURTI, U; SANDBERG, A. A et al.Cancer genetics and cytogenetics. 1991, Vol 53, Num 2, pp 199-203, issn 0165-4608Article

Rapid RFLP screening using DNA from complete hydatidiform molesLITT, M; BUDER, A; SURTI, U et al.Nucleic acids research. 1989, Vol 17, Num 1, issn 0305-1048, 464 (1 p.)Article

Effect of hydatidiform molar vesicular fluid on blood coagulationKAPLAN, S. S; SZULMAN, A. E; SURTI, U et al.American journal of obstetrics and gynecology. 1985, Vol 153, Num 6, pp 703-707, issn 0002-9378Article

Morphologic anomalies in triploid liveborn fetusesDOSHI, N; SURTI, U; SEULMAN, A. E et al.Human pathology. 1983, Vol 14, Num 8, pp 716-723, issn 0046-8177Article

Comparative study of primary and recurrent ovarian serous carcinomas: comparative genomic hybridization analysis with a potential application for prognosisHU, J; KHANNA, V; JONES, M. W et al.Gynecologic oncology (Print). 2003, Vol 89, Num 3, pp 369-375, issn 0090-8258, 7 p.Article

Three cases of tetrasomy 9pDHAUDHA, S; HOGGE, W. A; SURTI, U et al.American journal of medical genetics. 2002, Vol 113, Num 4, pp 375-380, issn 0148-7299, 6 p.Article

Genetics and biology of human ovarian teratomas. I, Cytogenetic analysis and mechanism of originSURTI, U; HOFFNER, L; CHAKRAVARTI, A et al.American journal of human genetics. 1990, Vol 47, Num 4, pp 635-643, issn 0002-9297, 9 p.Article

Cytogenetic and histologic correlation of peripheral nerve sheath tumors of soft tissueRAO, U. N. M; SURTI, U; HOFFNER, L et al.Cancer genetics and cytogenetics. 1996, Vol 88, Num 1, pp 17-25, issn 0165-4608Article

Apparently balanced t(1;7)(q21.3;q34) in an infant with Coffin-Siris syndromeMCPHERSON, E. W; LANERI, G; CLEMENS, M. M et al.American journal of medical genetics. 1997, Vol 71, Num 4, pp 430-433, issn 0148-7299Article

Small marker X chromosomes lack the X inactivation center : implications for karyotype/phenotype correlationsWOLFF, D. J; BROWN, C. J; SCHWARTZ, S et al.American journal of human genetics. 1994, Vol 55, Num 1, pp 87-95, issn 0002-9297Article

A hypervariable region at the D19S11 locusBUROKER, N. E; BUFTON, L; SURTI, U et al.Human genetics. 1987, Vol 76, Num 1, pp 90-95, issn 0340-6717Article

Tetraploid partial hydatidiform moles: two cases with a triple paternal contribution and a 92, XXXY karyotypeSURTI, U; SZULMAN, A. E; WAGNER, K et al.Human genetics. 1986, Vol 72, Num 1, pp 15-21, issn 0340-6717Article

Molecular analysis of chromosome 7q21.3 in uterine leiomyoma : Analysis using markers with linkage to insulin resistanceSELL, S. M; ALTUNGOZ, O; PROWSE, A. A et al.Cancer genetics and cytogenetics. 1998, Vol 100, Num 2, pp 165-168, issn 0165-4608Article

Nongestational choriocarcinoma in the postpartum period : A case reportSURYANARAYAN, K; O'HANLAN, K. A; SURTI, U et al.Journal of pediatric hematology/oncology. 1998, Vol 20, Num 2, pp 169-173, issn 1077-4114Article

Genetics and biology of human ovarian teratomas. III: Cytogenetics and origins of malignant ovarian germ cell tumorsHOFFNER, L; SHEN-SCHWARZ, S; DEKA, R et al.Cancer genetics and cytogenetics. 1992, Vol 62, Num 1, pp 58-65, issn 0165-4608Article

Nonrandom cytogenetic changes in leiomyomas of the female genitourinary tract : a report of 35 casesKIECHLE-SCHWARZ, M; SREEKANTAIAH, C; BERGER, C. S et al.Cancer genetics and cytogenetics. 1991, Vol 53, Num 1, pp 125-136, issn 0165-4608, 12 p.Article

Cryptic duplication of 12q24.33 → qter in a child with angelman syndrome- : Simultaneous occurrence of two unrelated cytogenetic eventsSATHANOORI, M; HU, J; MURTHY, V et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 9, pp 985-994, issn 1552-4825, 10 p.Article