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FONG KM
KODAGODA D
MCINTIRE D
HUNG J
TONK V
MINNA JD
GAZDAR AF
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KEUNG YK
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Citation: Yk. Keung et al., UNUSUAL PRESENTATION OF MULTIPLE-MYELOMA WITH JUMPING TRANSLOCATION INVOLVING 1Q21 - A CASE-REPORT AND REVIEW OF THE LITERATURE, Cancer genetics and cytogenetics, 106(2), 1998, pp. 135-139
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Authors:
GAZDAR AF
KURVARI V
VIRMANI A
GOLLAHON L
SAKAGUCHI M
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KODAGODA D
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WISTUBA II
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TONK V
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Citation: Af. Gazdar et al., CHARACTERIZATION OF PAIRED TUMOR AND NONTUMOR CELL-LINES ESTABLISHED FROM PATIENTS WITH BREAST-CANCER, International journal of cancer, 78(6), 1998, pp. 766-774
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STASTNY VA
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SCHNEIDER NR
WISTUBA II
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GAZDAR AF
Citation: Ge. Tomlinson et al., CHARACTERIZATION OF A BREAST-CANCER CELL-LINE DERIVED FROM A GERM-LINE BRCA1 MUTATION CARRIER, Cancer research, 58(15), 1998, pp. 3237-3242
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SHANKAR V
PICHAN P
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TONK V
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Citation: V. Shankar et al., CHROMOSOMAL LOCALIZATION OF A HUMAN MUCIN GENE (MUC8) AND CLONING OF THE CDNA CORRESPONDING TO THE CARBOXY-TERMINUS, American journal of respiratory cell and molecular biology, 16(3), 1997, pp. 232-241
Citation: V. Tonk et J. Krishna, CASE-REPORT - DE-NOVO INHERITED 18P DELETION IN A MOTHER-FETUS PAIR WITH EXTREMELY VARIABLE EXPRESSION, CONFIRMED BY FLUORESCENCE IN-SITU HYBRIDIZATION (FISH) ANALYSIS, European journal of obstetrics, gynecology, and reproductive biology, 73(2), 1997, pp. 193-196
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KEUNG YK
COBOS E
MORGAN D
WHITEHEAD RP
TONK V
Citation: Yk. Keung et al., DOUBLE MINUTE CHROMOSOMES AND MYELODYSPLASTIC SYNDROME - A CASE-REPORT AND LITERATURE-REVIEW, Cancer genetics and cytogenetics, 97(2), 1997, pp. 94-96
Citation: J. Krishna et al., INTERSTITIAL DELETION OF LONG ARM OF CHROMOSOME NO-5 WITH GROWTH-HORMONE DEFICIENCY - AN EMERGING SYNDROME, Clinical genetics, 51(1), 1997, pp. 48-51
Citation: A. Perry et al., INTERPHASE CYTOGENETIC (IN-SITU HYBRIDIZATION) ANALYSIS OF ASTROCYTOMAS USING ARCHIVAL, FORMALIN-FIXED, PARAFFIN-EMBEDDED TISSUE AND NONFLUORESCENT LIGHT-MICROSCOPY, American journal of clinical pathology, 108(2), 1997, pp. 166-174
Citation: Yk. Keung et al., DEVELOPMENT OF MINIMALLY DIFFERENTIATED ACUTE MYELOBLASTIC-LEUKEMIA WITH NOVEL ISOCHROMOSOME 18P AND ANTECEDENT APLASTIC-ANEMIA, Cancer genetics and cytogenetics, 92(1), 1996, pp. 1-3
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MORGAN DL
DUNN DM
COBOS E
KEUNG YK
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TONK V
Citation: Dl. Morgan et al., TRANSLOCATION T(15-17) IN ACUTE MYELOGENOUS LEUKEMIA WITH ATYPICAL MEGAKARYOBLASTIC FEATURES - DIAGNOSTIC, CLINICAL, AND THERAPEUTIC IMPLICATIONS, Cancer genetics and cytogenetics, 92(1), 1996, pp. 50-53
Authors:
LOWICHIK A
SCHNEIDER NR
TONK V
ANSARI MQ
TIMMONS CF
Citation: A. Lowichik et al., REPORT OF A COMPLEX KARYOTYPE IN RECURRENT METASTATIC FIBROLAMELLAR HEPATOCELLULAR-CARCINOMA AND A REVIEW OF HEPATOCELLULAR-CARCINOMA CYTOGENETICS, Cancer genetics and cytogenetics, 88(2), 1996, pp. 170-174
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TONK V
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CHRISTIAN SL
KUBOTA T
LEDBETTER DH
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Citation: V. Tonk et al., ROBERTSONIAN (15Q-15Q) TRANSLOCATION IN A CHILD WITH ANGELMAN-SYNDROME - EVIDENCE OF UNIPARENTAL DISOMY, American journal of medical genetics, 66(4), 1996, pp. 426-428
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TONK V
SCHNEIDER R
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MAO JI
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Citation: V. Tonk et al., IDENTIFICATION AND MOLECULAR CONFIRMATION OF A SMALL CHROMOSOME 10Q DUPLICATION [DIR DUP(10)(Q24.2-]Q24.3)] INHERITED FROM A MOTHER MOSAIC FOR THE ABNORMALITY, American journal of medical genetics, 61(1), 1996, pp. 16-20
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BERNINI JC
TONK V
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TIMMONS CF
Citation: A. Lowichik et al., RELAPSE OF PRECURSOR B-CELL ACUTE LYMPHOBLASTIC-LEUKEMIA AS AN ISOLATED CENTRAL-NERVOUS-SYSTEM MASS LESION 9 YEARS AFTER INITIAL DIAGNOSIS, Medical and pediatric oncology, 26(2), 1996, pp. 129-134
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TONK V
WILSON KS
TIMMONS CF
SCHNEIDER NR
TOMLINSON GE
Citation: V. Tonk et al., RENAL-CELL CARCINOMA WITH TRANSLOCATION (X-1) - FURTHER EVIDENCE FOR A CYTOGENETICALLY DEFINED SUBTYPE, Cancer genetics and cytogenetics, 81(1), 1995, pp. 72-75
Authors:
KULHARYA AS
MABERRY M
KUKOLICH MK
DAY DW
SCHNEIDER NR
WILSON GN
TONK V
Citation: As. Kulharya et al., INTERSTITIAL DELETIONS 4Q21.1Q25 AND 4Q25Q27 - PHENOTYPIC VARIABILITYAND RELATION TO RIEGER ANOMALY, American journal of medical genetics, 55(2), 1995, pp. 165-170
Citation: A. Haider et al., CLINICAL AND CYTOGENETIC STUDIES IN TURNER SYNDROME MOTHER AND HER 2 DAUGHTERS WITH DEL(X)(P21.2) INHERITED FROM A MOTHER MOSAIC FOR THE ABNORMALITY, Pediatric research, 37(4), 1995, pp. 90-90
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TONK V
WYANDT HE
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SKARE J
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HADDAD B
MILUNSKY A
Citation: V. Tonk et al., CYTOGENETIC AND MOLECULAR CYTOGENETIC STUDIES OF A CASE OF INTERSTITIAL DELETION OF PROXIMAL 15Q, Clinical genetics, 48(3), 1995, pp. 151-155
Citation: V. Tonk et al., COMPARATIVE-ANALYSIS OF THE KARYOTYPIC STABILITY IN LYMPHOBLASTOID CELL-LINES REPRESENTING APPARENTLY NORMAL CONTROLS, ROBERTS-SYNDROME, AND BLOOM-SYNDROME, American journal of human genetics, 57(4), 1995, pp. 724-724
Authors:
MIRZAYANS F
TONK V
KUKOLICH MK
PEARCE WG
WALTER MA
Citation: F. Mirzayans et al., DEFINITION OF A 14 CM CRITICAL REGION FOR AXENFELD-RIEGER SYNDROME ATCHROMOSOME 4Q25-27, American journal of human genetics, 57(4), 1995, pp. 1137-1137