A. Meloni

发表

FISH studies of urinary cells of patients with bladder cancer.

A. Peier, A. Sandberg, A. Meloni, 1995, Urologic oncology.

Translocation (X;1) in papillary renal cell carcinoma. A new cytogenetic subtype.

A. Sandberg, J. Pontes, A. Meloni, 1993, Cancer genetics and cytogenetics.

Sublocalization of the synovial sarcoma-associated t(X;18) chromosomal breakpoint in Xp11.2 using cosmid cloning and fluorescence in situ hybridization.

R. Sinke, A. Sandberg, M. Geraghty, 1993, Oncogene.

Unbalanced chromosomal translocation, der(17)t(13;17)(q14;p11) in a solid and cystic papillary epithelial neoplasm of the pancreas.

A. Sandberg, G. Lauwers, J. Stone, 1996, The American journal of surgical pathology.

Overrepresentation of chromosome 12p sequences and karyotypic evolution in i(12p)-negative testicular germ-cell tumors revealed by fluorescence in situ hybridization.

R. Sinke, A. Sandberg, R. Suijkerbuijk, 1993, Cancer genetics and cytogenetics.

Localization of X chromosome short arm markers relative to synovial sarcoma- and renal adenocarcinoma-associated translocation breakpoints

D. Weghuis, R. Sinke, W. Berger, 1993, Human Genetics.

Distinct Xp11.2 breakpoint regions in synovial sarcoma revealed by metaphase and interphase FISH: relationship to histologic subtypes.

E. van den Berg, A. Sandberg, L. Kindblom, 1994, Cancer genetics and cytogenetics.

Identification of a yeast artificial chromosome that spans the human papillary renal cell carcinoma-associated t(X;1) breakpoint in Xp11.2.

A. Monaco, R. Sinke, A. Sandberg, 1993, Cancer genetics and cytogenetics.

Involvement of chromosome 7 in Wilms tumor.

A. Peier, A. Sandberg, A. Meloni, 1995, Cancer genetics and cytogenetics.

Deletion (5q) in a desmoid tumor of a patient with Gardner's syndrome.

H. Lynch, A. Sandberg, A. Meloni, 1994, Cancer genetics and cytogenetics.

Cytogenetic studies in endometriosis tissue.

A. Sandberg, A. Meloni, A. Dangel, 1994, Cancer genetics and cytogenetics.

Cytogenetic findings in a metastatic renal cell carcinoma.

P. Carroll, A. Peier, S. Leong, 1995, Cancer genetics and cytogenetics.

Reviews of chromosome studies in urological tumors. III. Cytogenetics and genes in testicular tumors.

A. Sandberg, R. Suijkerbuijk, A. Meloni, 1996, The Journal of urology.

t(16;21)(p11.2;q22): a recurrent primary rearrangement in ANLL.

A. Meloni, R. Lemons, R. Morgan, 1991, Cancer genetics and cytogenetics.

Leptomeningeal metastasis from a paraspinal rhabdomyosarcoma with a der(13)t(1;13)(q23;q32) in a 14-month-old boy.

A. Sandberg, A. Meloni, R. Oseas, 1997, Cancer genetics and cytogenetics.

Cytogenetic findings‐in 19 malignant bone tumors

Y. Ozisik, A. Peier, S. Leong, 1994, Cancer.

Reviews on chromosome studies in urological tumors. I. Renal tumors.

A. Sandberg, J. Bridge, A. Meloni, 1992, The Journal of urology.

del(6q) as a possible primary change in malignant mesothelioma.

F. Li, A. Sandberg, A. Meloni, 1992, Cancer genetics and cytogenetics.

Two discrete regions of deletion at 7q in uterine leiomyomas

U. Surti, R. Ferrell, A. Sandberg, 1997, Genes, chromosomes & cancer.

Molecular and cytogenetic analysis of chromosome 7 in uterine leiomyomas

U. Surti, R. Ferrell, A. Sandberg, 1995, Genes, chromosomes & cancer.

Molecular analysis of chromosome 7q21.3 in uterine leiomyoma: analysis using markers with linkage to insulin resistance.

U. Surti, A. Sandberg, A. Meloni, 1998, Cancer genetics and cytogenetics.

Trisomies 8 and 20 characterize a subgroup of benign fibrous lesions arising in both soft tissue and bone.

J. Lynch, G. Maale, J. Neff, 1999, The American journal of pathology.

Deletion 5q in desmoid tumor and fluorescence in situ hybridization for chromosome 8 and/or 20 copy number.

A. Sandberg, J. Neff, J. Bridge, 1996, Cancer genetics and cytogenetics.

A new approach in the diagnosis and follow-up of bladder cancer. FISH analysis of urine, bladder washings, and tumors.

A. Peier, A. Sandberg, I. Powell, 1993, Cancer genetics and cytogenetics.

Cytogenetic findings in 21 malignant melanomas.

Y. Ozisik, A. Peier, S. Leong, 1994, Cancer genetics and cytogenetics.

Deletion of chromosome 13 in osteosarcoma secondary to irradiation.

Y. Ozisik, M. Zalupski, A. Sandberg, 1993, Cancer genetics and cytogenetics.

Deletion 1p in a low-grade chondrosarcoma in a patient with Ollier disease.

C. H. Bush, Y. Ozisik, A. Sandberg, 1998, Cancer genetics and cytogenetics.

Deletion 7q22 in uterine leiomyoma. A cytogenetic review.

U. Surti, Y. Ozisik, A. Sandberg, 1993, Cancer genetics and cytogenetics.

Inversion (X)(p22q13) in a uterine leiomyoma.

U. Surti, Y. Ozisik, A. Sandberg, 1992, Cancer genetics and cytogenetics.

-Y,-1 as recurrent anomaly in oncocytoma.

A. Sandberg, R. White, A. Meloni, 1992, Cancer genetics and cytogenetics.

Analysis of 3p allelic loss in papillary and nonpapillary renal cell carcinomas. Correlation with tumor karyotypes.

M. Hughson, A. Sandberg, A. Meloni, 1996, Cancer genetics and cytogenetics.

Identification of a yeast artificial chromosome (YAC) that spans the papiliary renal cell carcinoma-associated t(X;1)(p11;q21) breakpoint

A. Monaco, A. Sandberg, R. Suijkerbuijk, 1993 .

Trisomy 5 in long-term cultures from bone marrow of patients with solid tumors.

Y. Ozisik, A. Peier, A. Sandberg, 1994, Cancer genetics and cytogenetics.

Translocation (X;1)(p11.2;q21). A subtype of renal adenocarcinomas.

A. Sandberg, J. Pontes, A. Meloni, 1992, Cancer genetics and cytogenetics.

Characterization of unusual marker chromosomes in testicular tumors by fluorescence in situ hybridization

A. Sandberg, R. D. White, A. Meloni, 1991 .

Misexpression of disrupted HMGI architectural factors activates alternative pathways of tumorigenesis.

K. Chada, A. Sandberg, A. Tkachenko, 1997, Cancer research.

Hepatic undifferentiated (embryonal) sarcoma arising in a mesenchymal hamartoma.

G. Lauwers, A. Meloni, W. Donnelly, 1997, The American journal of surgical pathology.

Trisomy 10 in renal cell carcinoma.

A. Sandberg, J. Pontes, A. Meloni, 1991, Cancer genetics and cytogenetics.

Translocation (6;10)(p21;q22) in uterine leiomyomas.

U. Surti, Y. Ozisik, A. Sandberg, 1995, Cancer genetics and cytogenetics.

Chromosome abnormalities in breast fibroadenomas.

Y. Ozisik, A. Peier, A. Sandberg, 1994, Cancer genetics and cytogenetics.

Chromosome 7 biclonality in uterine leiomyoma.

U. Surti, Y. Ozisik, A. Sandberg, 1993, Cancer genetics and cytogenetics.

Uterine Leiomyomas: Cytogenetic and Histologic Profile

U. Surti, A. Sandberg, A. Meloni, 1992, Obstetrics and gynecology.

Involvement of 10q22 in leiomyoma.

U. Surti, Y. Ozisik, A. Sandberg, 1993, Cancer genetics and cytogenetics.

Deletion of both chromosome 7 homologues in leiomyoma.

U. Surti, A. Peier, A. Sandberg, 1995, Cancer genetics and cytogenetics.

Spontaneous expression of the chromosome fragile site at 10q23 in leiomyoma.

U. Surti, Y. Ozisik, A. Sandberg, 1994, Cancer genetics and cytogenetics.

Cloning of a breakpoint cluster region on chromosome 14 in uterine leiomyoma.

L. Deaven, T. Smolarek, A. Sandberg, 1998, Cancer letters.

Cytogenetic changes in ovarian mucinous cystadenocarcinoma of low malignant potential with persistent pseudomyxoma peritonei.

A. Sandberg, A. Meloni, S. Vasilev, 1995, Cancer genetics and cytogenetics.

Involvement of 10q22 and 11q13 in hibernoma.

C. H. Bush, A. Sandberg, S. Spanier, 1994, Cancer genetics and cytogenetics.

Deletion 6q in three cases of mixed-type liposarcoma in addition to t(12;16)(q13;p11)

A. Peier, M. Zalupski, A. Sandberg, 1995, Cancer genetics and cytogenetics.

Cytogenetic findings in a case of angiomyxoma of the vaginal wall

G. Moore, A. Sandberg, A. Meloni, 1995 .

Renal cell carcinoma of end-stage renal disease: a histopathologic and molecular genetic study.

L. Schmidt, B. Zbar, M. Hughson, 1996, Journal of the American Society of Nephrology : JASN.

FISH studies on the Y chromosome in male urinary cells.

A. Sandberg, A. Meloni, J. Betz, 1996, Cancer genetics and cytogenetics.

Clear-cell and papillary carcinoma of the kidney: an analysis of chromosome 3, 7, and 17 abnormalities by microsatellite amplification, cytogenetics, and fluorescence in situ hybridization.

M. Hughson, S. Bigler, K. Dickman, 1998, Cancer genetics and cytogenetics.

Two cases of low-grade gastric leiomyosarcoma with monosomy 14 as the only change.

A. Sandberg, G. Lauwers, A. Meloni, 1996, Cancer genetics and cytogenetics.

Fine mapping of the human renal oncocytoma-associated translocation (5;11)(q35;q13) breakpoint.

E. van den Berg, D. Weghuis, R. Sinke, 1997, Cancer genetics and cytogenetics.

Renal cell carcinoma in an end-stage kidney of a patient with a functional transplant: cytogenetic and molecular genetic findings.

M. Hughson, A. Sandberg, A. Meloni, 1996, Cancer genetics and cytogenetics.

Deletion of chromosome 13 in leiomyomas of the uterus.

U. Surti, A. Sandberg, A. Meloni, 1991, Cancer genetics and cytogenetics.

Cytogenetic findings in a symplastic leiomyoma.

U. Surti, Y. Ozisik, A. Sandberg, 1993, Cancer genetics and cytogenetics.

Cytogenetic findings in typical and atypical meningioma.

R. Lewin, A. Meloni, M. Erling, 1991, Cancer genetics and cytogenetics.

Misexpression of disrupted HMGI architectural factors activates alternative pathways of tumorigenesis.

K. Chada, A. Tkachenko, A. Meloni, 1997, Cancer research.

Uterine Leiomyomas: Cytogenetic and Histologic Profile

U. Surti, A. Sandberg, A. Meloni, 1992, Obstetrics and gynecology.