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I. Halbrecht

Tel Aviv University

109

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1164

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Interpretation of a marker chromosome 17p in multiple myeloma

2009 Hereditas
- F. Shabtai
- I. Halbrecht
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Citations (6)
Bloom's syndrome, missing Y, hypogonadism and cancer

2008 Clinical Genetics
- Fiorella Shabtai
- I. Halbrecht
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Citations (3)
Human chromosome polymorphism and congenital malformations.

2008 Clinical Genetics
- I. Halbrecht
- Fiorella Shabtay
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Citations (34)
Risk of malignancy and chromosomal polymorphism: a possible mechanism of association.

2008 Clinical Genetics
- Florella Shabtai
- I. Halbrecht
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Citations (61)
New anomalies found in the 11q-syndrome.

2008 Clinical Genetics
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Citations (16)
Isochromosome Y [46, X, i(Yq)] and female phenotype

2008 Clinical Genetics
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Aplastic anemia followed by leukemia in congenital trisomy 8 mosaicism:Ultrastructural studies of polymorphonuclear cells in peripheral blood

2008 Clinical Genetics
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Familial syndrome with some features of the Langer‐Giedion syndrome, and paracentric inversion of chromosome 8, inv 8 (q11.23<q21.1)

2008 Clinical Genetics
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Triploidy 69, XXX in a stillborn girl

2008 Clinical Genetics
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49,XYYYY. A case report.

2008 Clinical Genetics
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Citations (32)