C. Berger

发表

Review of chromosome studies in urological tumors. II. Cytogenetics and molecular genetics of bladder cancer.

A. Sandberg, C. Berger, 1994, The Journal of urology.

Translocation t(3;8)(p14.2;q24.1) in renal cell carcinoma affects expression of the common fragile site at 3p14(FRA3B) in lymphocytes.

F. Hecht, T. Glover, F. Li, 1988, Cancer genetics and cytogenetics.

Identification of masked and variant Ph (complex type) translocations in CML and classic Ph in AML and ALL by fluorescence in situ hybridization with the use of bcr/abl cosmid probes.

J. Stone, R. Morgan, A. Sandberg, 1993, Cancer genetics and cytogenetics.

Chromosome change in transitional cell carcinoma of ureter.

F. Hecht, A. Sandberg, F. Haddad, 1986, Cancer genetics and cytogenetics.

Analysis of a giant marker chromosome in a well-differentiated liposarcoma using cytogenetics and fluorescence in situ hybridization.

J. Davis, S. Leong, A. Sandberg, 1992, Cancer genetics and cytogenetics.

Ring chromosome in a dermatofibrosarcoma protuberans.

S. Leong, A. Sandberg, J. Davis, 1992, Cancer genetics and cytogenetics.

Loss of common 3p14 fragile site expression in renal cell carcinoma with deletion breakpoint at 3p14.

F. Hecht, E. Tajara, B. Hecht, 1988, Cancer genetics and cytogenetics.

Histiocytic lymphoma cell lines: immunologic and cytogenetic studies.

F. Hecht, B. Hecht, A. Epstein, 1985, Cancer genetics and cytogenetics.

Use of novel chemical supplements in the establishment of three human malignant lymphoma cell lines (NU‐DHL‐1, NUDUL‐1, and NU‐AMB‐1) with chromosome 14 translocations

B. Hecht, A. Epstein, D. Variakojis, 1985, International journal of cancer.

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

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

Direct prenatal chromosome diagnosis of a malignancy.

F. Hecht, H. Finberg, B. Hecht, 1984, Cancer genetics and cytogenetics.

DNA polymerase α inhibition by aphidicolin induces gaps and breaks at common fragile sites in human chromosomes

T. Glover, C. Berger, Jane Coyle, 2004, Human Genetics.

Familial double testicular tumors: identical chromosome changes in seminoma and embryonal carcinoma of the same testis.

M. Nathan, A. Sandberg, F. Haddad, 1988, The Journal of urology.

inv(12)(p11.2q13) in an endometrial polyp.

A. Sandberg, T. Walter, H. Decker, 1989, Cancer genetics and cytogenetics.

Isolation of a yeast artificial chromosome clone that spans the (12;16) translocation breakpoint characteristic of myxoid liposarcoma.

R. Gemmill, A. Sandberg, J. Trent, 1992, Cancer genetics and cytogenetics.

Nonradioactive in situ hybridization. A rapid approach for the identification of marker chromosomes: study of a case of acute leukemia with a Yq specific DNA probe.

B. Wullich, R. Morgan, A. Sandberg, 1991, Cancer genetics and cytogenetics.

Detection of monosomy in interphase nuclei and identification of marker chromosomes using biotinylated alpha-satellite DNA probes.

H. Fiebig, A. Sandberg, M. Kiechle‐Schwarz, 1991, Cancer genetics and cytogenetics.

Presence of telomeric sequences on deleted chromosomes and their absence on double minutes in cell line HL-60.

R. Morgan, T. Furuya, A. Sandberg, 1993, Cancer genetics and cytogenetics.

The cytogenetics of renal tumors. Where do we stand, where do we go?

A. Sandberg, T. Walter, C. Berger, 1989, Cancer genetics and cytogenetics.

Aneuploidy in recurrent spontaneous aborters: the tendency to parental nondisjunction

B. Hecht, C. Berger, Frederick Hecht, 1984, Clinical genetics.

Nonrandom cytogenetic changes in leiomyomas of the female genitourinary tract. A report of 35 cases.

U. Surti, A. Sandberg, C. Sreekantaiah, 1991, Cancer genetics and cytogenetics.

Nonrandom cytogenetic changes in leiomyomas of the female genitourinary tract.

U. Surti, A. Sandberg, C. Sreekantaiah, 1991 .

Cytogenetic findings in nine leiomyomas of the uterus.

A. Sandberg, C. Sreekantaiah, M. Medchill, 1990, Cancer genetics and cytogenetics.

Rearrangement of band 10q22 in leiomyoma and leiomyosarcoma of the uterus.

U. Surti, A. Sandberg, M. Kiechle‐Schwarz, 1990, Cancer genetics and cytogenetics.

Cluster of trisomy 12 to tumors of the female genitourinary tract.

A. Sandberg, C. Sreekantaiah, M. Kiechle‐Schwarz, 1991, Cancer genetics and cytogenetics.

Application of fluorescence in situ hybridization in hematological disorders.

Z Chen, A A Sandberg, R Morgan, 1992, Cancer genetics and cytogenetics.

Chromosome analysis in hematologic disorders. The leukemias.

F. Hecht, B. Hecht, A. Sandberg, 1984, The American journal of medicine.

DNA demethylation induced by 5-azacytidine does not affect fragile X expression.

T. Glover, R. Gemmill, J. Coyle-Morris, 1986, American journal of human genetics.

Chromosomes in kidney, ureter, and bladder cancer.

F. Hecht, B. Hecht, A. Sandberg, 1986, Cancer genetics and cytogenetics.

Cytogenetic subtype involving chromosome 13 in lipoma. Report of three cases.

S. Leong, A. Sandberg, C. Karakousis, 1989, Cancer genetics and cytogenetics.

CD5- mantle cell lymphoma.

C. D. Wu, W. Gorczyca, P. Tsang, 2002, American journal of clinical pathology.

Trisomy 2 in proliferative fasciitis.

A. Sandberg, J. Neff, J. Bridge, 1992, Cancer genetics and cytogenetics.

CAR-HEMATOTOX: A model for CAR T-cell related hematological toxicity in relapsed/refractory large B-cell lymphoma.

E. Hoster, G. Salles, A. Mackensen, 2021, Blood.

Chromosomes 17 and 22 involved in marker formation in neurofibrosarcoma in von Recklinghausen disease

S. Leong, A. Sandberg, L. Cannizzaro, 1990, Human Genetics.

Cytoplasmic Immunoglobulin Fluorescence In Situ Hybridization (cIg FISH) Enhances the Quantitative Detection of Chromosome Abnormalities In Plasma Cell Neoplasms Compared to Conventional FISH

S. Jagannath, Hai-Su Yang, T. Scholl, 2010 .

Adenocarcinoma of the gallbladder: chromosome abnormalities in a genetic form of cancer.

F. Hecht, B. Hecht, A. Sandberg, 1983, Cancer genetics and cytogenetics.