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Dvora Klar

Tel Aviv University

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Co-Authors

Fiorella Shabtai

Tel Aviv University

I. Halbrecht

Tel Aviv University

J. Hart

Regional Medical Center

Isaac Halbrecht

Tel Aviv University

Raphael Reiss

University of Tübingen

Jacob Hart

Wilson College

Ahud Sternberg

Technion – Israel Institute of Technology

U Lewinski

Rabin Medical Center

M Djaldetti

Tel Aviv University

R. Nissimov

Lev Hasharon Hospital

Cooperative Institutions

Tel Aviv University

Lev Hasharon Hospital

Rabin Medical Center

Meir Medical Center

Institute for Human Reproduction

Hadassah Medical Center

Technion – Israel Institute of Technology

Hillel Yaffe Medical Center

Loewenstein Hospital Rehabilitation Center

University of Washington

Author Statistics

Papers

Citation

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Research Field

Different inducibility and possible significance of several concomitant ?fragile sites? in two brothers

Human Genetics (1986)

Fiorella Shabtai Jerome Orlin J. Hart I. Halbrecht Dvora Klar

Chromosomal fragile site

Human genetics

10.1007/bf00278791

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Citations (9)

Non-random chromosomal aberrations in a complex leukaemic clone of a Bloom's syndrome patient

Human Genetics (1988)

Fiorella Shabtai U Lewinski A. Meroz Dvora Klar M Djaldetti

Bloom syndrome

Bloom

Human genetics

Metabolic disease

clone (Java method)

10.1007/bf01790108

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Citations (6)

Familial fragile 8q22 involved as a cancer breakpoint in cells of a large bowel tumor

Cancer Genetics and Cytogenetics (1988)

Fiorella Shabtai Ahud Sternberg Dvora Klar Isaac Halbrecht Raphael Reiss

Chromosomal fragile site

Breakpoint

10.1016/0165-4608(88)90018-0

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Citations (11)

Cytogenetic study of patients with carcinoma of the colon and rectum: Particular C-band variants as possible markers for cancer proneness

Cancer Genetics and Cytogenetics (1985)

Fiorella Shabtai Elie Antebi Dvora Klar D Kimchi J. Hart

10.1016/0165-4608(85)90189-x

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Citations (27)

A new familial ?fragile site? on chromosome 16 (q23-24). Cytogenetic and clinical considerations

Human Genetics (1983)

Fiorella Shabtai Dvora Klar R. Nissimov D. Vardimon J. Hart

Chromosomal fragile site

Human genetics

Metabolic disease

10.1007/bf00279409

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Citations (17)

Familial syndrome with some features of the Langer‐Giedion syndrome, and paracentric inversion of chromosome 8, inv 8 (q11.23<q21.1)

Clinical Genetics (1985)

F. Shabta Uri Sandowski R. Nissimov Dvora Klar I. Halbrecht

A family is reported with an autosomal dominant inherited syndrome presenting some of the typical features of the tricho‐rhino‐phalangeal syndrome type II (TRP II) or Langer‐Giedion syndrome. The critical region for the expression of the syndrome seems to be at band 8q24.1. In the affected members of the family reported here, anomaly of chromosome 8 was noted, involving however the proximal part of the 8 long arm, which was interpreted as a paracentric inversion. Whether the anomaly is causally or only casually related to the syndrome is a matter of discussion.

Chromosomal inversion

10.1111/j.1399-0004.1985.tb02045.x

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Citations (13)

Chromosome 17 has a real fragile site at p12

Human Genetics (1982)

Fiorella Shabtai Dvora Klar I. Halbrecht

Chromosomal fragile site

Human genetics

Metabolic disease

10.1007/bf00274215

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Citations (17)

Familial fragile site found at the cancer breakpoint (1)(q32)

Human Genetics (1986)

Fiorella Shabtai J. Hart Dvora Klar I. Halbrecht

Chromosomal fragile site

Breakpoint

Human genetics

Metabolic disease

10.1007/bf00401234

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Citations (12)

Involvement of chromosome 22 in a Merkel cell carcinoma in a patient with a previous meningioma

Cancer Genetics and Cytogenetics (1989)

Fiorella Shabtai A Sternberg Dvora Klar Raphael Reiss I. Halbrecht

Merkel cell

10.1016/0165-4608(89)90163-5

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Citations (21)

Familial fragility on chromosome 16 (Fra 16q22) enhanced by both interferon and distamycin A

Human Genetics (1983)

Fiorella Shabtai Dvora Klar Shlomo Bichacho J. Hart I. Halbrecht

Chromosomal fragile site

Human genetics

Metabolic disease

10.1007/bf00274759

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Citations (15)