Authors:
ROBSON WLM
SHASHI V
NAGARAJ S
NORGAARD JP
Citation: Wlm. Robson et al., WATER-INTOXICATION IN A PATIENT WITH THE PRADER-WILLI-SYNDROME TREATED WITH DESMOPRESSIN FOR NOCTURNAL ENURESIS, The Journal of urology, 157(2), 1997, pp. 646-647
Authors:
GAFFEY MJ
FRIERSON HF
IEZZONI JC
MILLS SE
CLEMENT PB
GERSELL DJ
SHASHI V
VONKAPHERR C
YOUNG RH
Citation: Mj. Gaffey et al., OVARIAN GRANULOSA-CELL TUMORS WITH BIZARRE NUCLEI - AN IMMUNOHISTOCHEMICAL ANALYSIS WITH FLUORESCENCE IN-SITU HYBRIDIZATION DOCUMENTING TRISOMY-12 IN THE BIZARRE COMPONENT (VOL 9, PG 308, 1996), Modern pathology, 9(7), 1996, pp. 803-803
Authors:
GAFFEY MJ
FRIERSON HF
IEZZONI JC
MILLS SE
CLEMENT PB
GERSELL DJ
SHASHI V
VONKAPHERR C
YOUNG RH
Citation: Mj. Gaffey et al., OVARIAN GRANULOSA-CELL TUMORS WITH BIZARRE NUCLEI - AN IMMUNOHISTOCHEMICAL ANALYSIS, Modern pathology, 9(3), 1996, pp. 308-315
Authors:
SHASHI V
GOLDEN WL
VONKAPHERR C
WILSON WG
Citation: V. Shashi et al., CONSTELLATION OF CONGENITAL-ABNORMALITIES IN AN INFANT - A NEW SYNDROME OR TISSUE-SPECIFIC MOSAICISM FOR TRISOMY-18, American journal of medical genetics, 62(1), 1996, pp. 38-41
Authors:
SHASHI V
GOLDEN WL
ALLINSON PS
BLANTON SH
VONKAPHERR C
KELLY TE
Citation: V. Shashi et al., MOLECULAR ANALYSIS OF RECOMBINATION IN A FAMILY WITH DUCHENNE MUSCULAR-DYSTROPHY AND A LARGE PERICENTRIC X-CHROMOSOME INVERSION, American journal of human genetics, 58(6), 1996, pp. 1231-1238
Authors:
SCHNEIDER BF
VANDENBERG SR
SUDDUTH KW
VONKAPHERR C
SHASHI V
GOLDEN WL
Citation: Bf. Schneider et al., STRUCTURAL ABNORMALITIES OF CHROMOSOME-14 IN MENINGIOMAS - EVIDENCE FOR A PROGRESSION GENE, Cytogenetics and cell genetics, 69(1-2), 1995, pp. 124-124
Authors:
SCHNEIDER BF
SHASHI V
VONKAPHERR C
GOLDEN WL
Citation: Bf. Schneider et al., LOSS OF CHROMOSOME-22 AND CHROMOSOME-14 IN THE MALIGNANT PROGRESSION OF MENINGIOMAS - A COMPARATIVE-STUDY OF FLUORESCENCE IN-SITU HYBRIDIZATION (FISH) AND STANDARD CYTOGENETIC ANALYSIS, Cancer genetics and cytogenetics, 85(2), 1995, pp. 101-104
Citation: V. Shashi et al., ABSENT PITUITARY-GLAND IN 2 BROTHERS WITH AN ORAL-FACIAL-DIGITAL SYNDROME RESEMBLING OFDS-II AND OFDS-VI - A NEW-TYPE OF OFDS, American journal of medical genetics, 57(1), 1995, pp. 22-26
Authors:
GAFFEY MJ
FRIERSON HF
MILLS SE
CLEMENT PB
SHASHI V
IEZZONI JC
GERSELL DJ
YOUNG RH
Citation: Mj. Gaffey et al., OVARIAN GRANULOSA-CELL TUMORS WITH BIZARRE NUCLEI (GCT-BN) - AN IMMUNOHISTOCHEMICAL AND FLUORESCENCE IN-SITU HYBRIDIZATION (FISH) STUDY, Laboratory investigation, 72(1), 1995, pp. 90-90
Citation: V. Shashi et al., NEUROECTODERMAL (CHIME) SYNDROME - AN ADDITIONAL CASE WITH LONG-TERM FOLLOW-UP OF ALL REPORTED CASES, Journal of Medical Genetics, 32(6), 1995, pp. 465-469
Citation: V. Shashi et Js. Fryburg, VASCULAR RING LEADING TO TRACHEOESOPHAGEAL COMPRESSION IN A PATIENT WITH RUBINSTEIN-TAYBI SYNDROME, Clinical genetics, 48(6), 1995, pp. 324-327
Authors:
SHASHI V
GOLDEN WL
VONKAPHERR C
ANDERSEN WA
GAFFEY MJ
Citation: V. Shashi et al., INTERPHASE FLUORESCENCE IN-SITU HYBRIDIZATION FOR TRISOMY-12 ON ARCHIVAL OVARIAN SEX CORD-STROMAL TUMORS, Gynecologic oncology, 55(3), 1994, pp. 349-354
Citation: V. Shashi et al., DECREASED RECOMBINATION IN OOGENESIS IN A FAMILY WITH A LARGE PERICENTRIC X-CHROMOSOME INVERSION, Pediatric research, 35(4), 1994, pp. 10000154-10000154
Citation: V. Shashi et al., MALIGNANT RHABDOID TUMOR OF THE KIDNEY - INVOLVEMENT OF CHROMOSOME-22, Cytogenetics and cell genetics, 63(4), 1993, pp. 257-257
Authors:
GOLDEN WL
SHASHI V
VONKAPHERR C
SUDDUTH KW
SCHNEIDER BF
Citation: Wl. Golden et al., COMPARATIVE FLUORESCENT IN-SITU HYBRIDIZATION AND STANDARD CYTOGENETIC ANALYSIS IN MENINGIOMAS, American journal of human genetics, 53(3), 1993, pp. 302-302
Authors:
SHASHI V
GOLDEN WL
VONKAPHERR C
GAFFEY MJ
Citation: V. Shashi et al., INTERPHASE CYTOGENETIC ANALYSIS FOR TRISOMY-12 IN OVARIAN SEX CORD-STROMAL TUMORS, American journal of human genetics, 53(3), 1993, pp. 364-364
Authors:
WILSON WG
GOLDEN WL
VONKAPHERR C
SHASHI V
Citation: Wg. Wilson et al., FISH DETECTION OF TISSUE-SPECIFIC MOSAICISM FOR TRISOMY-18 IN AN INFANT WITH MULTIPLE CONGENITAL-ANOMALIES, American journal of human genetics, 53(3), 1993, pp. 627-627