Amiel A - Search Results

1

Application of comparative genomic hybridization in search for genetic aberrations in fibroadenomas of the breast.

Amiel A, Kaufman Z, Goldstein E, Bruchim RB, Kidron D, Gaber E, Fejgin MD. Amiel A, et al. Cancer Genet Cytogenet. 2003 Apr 15;142(2):145-8. doi: 10.1016/s0165-4608(02)00833-6. Cancer Genet Cytogenet. 2003. PMID: 12699893

2

Fluorescence in situ hybridization (FISH) for retrospective detection of trisomies 3 and 7 in multiple myeloma.

Dubinsky R, Amiel A, Manor Y, Radnay Y, Fejgin M, Ravid M, Lishner M. Dubinsky R, et al. Among authors: amiel a. Cancer Genet Cytogenet. 1995 Sep;83(2):115-8. doi: 10.1016/0165-4608(95)00018-k. Cancer Genet Cytogenet. 1995. PMID: 7553579

3

Fluorescence in situ hybridization for the detection of trisomies 8 and 9 in polycythemia vera.

Amiel A, Gaber E, Manor Y, Fejgin M, Joseph-Lerner N, Ravid M, Lishner M. Amiel A, et al. Cancer Genet Cytogenet. 1995 Feb;79(2):153-6. doi: 10.1016/0165-4608(94)00139-3. Cancer Genet Cytogenet. 1995. PMID: 7889510

4

Detection of bcl rearrangements in B-CLL by fluorescence in situ hybridization.

Amiel A, Lishner M, Lalkin A, Gaber E, Manor Y, Fejgin M, Yarkoni S, Ravid M. Amiel A, et al. Cancer Genet Cytogenet. 1994 Apr;73(2):165-8. doi: 10.1016/0165-4608(94)90203-8. Cancer Genet Cytogenet. 1994. PMID: 8174093

5

In situ hybridization: a simple and sensitive method for detection of trisomy 12 in chronic lymphocytic leukemia.

Lalkin A, Lishner M, Gaber E, Manor Y, Fejgin M, Ravid M, Amiel A. Lalkin A, et al. Among authors: amiel a. Cancer Genet Cytogenet. 1993 Oct 1;70(1):21-4. doi: 10.1016/0165-4608(93)90126-7. Cancer Genet Cytogenet. 1993. PMID: 8221608

6

Clinical detection of BCR-abl fusion by in situ hybridization in chronic myelogenous leukemia.

Amiel A, Yarkoni S, Fejgin M, Gaber E, Nagler A, Manor Y, Lishner M. Amiel A, et al. Cancer Genet Cytogenet. 1993 Jan;65(1):32-4. doi: 10.1016/0165-4608(93)90055-q. Cancer Genet Cytogenet. 1993. PMID: 8431913

7

The detection of trisomies 8 and 9 in patients with essential thrombocytosis by fluorescence in situ hybridization.

Elis A, Amiel A, Manor Y, Tangi I, Fejgin M, Lishner M. Elis A, et al. Among authors: amiel a. Cancer Genet Cytogenet. 1996 Nov;92(1):14-7. doi: 10.1016/s0165-4608(96)00115-x. Cancer Genet Cytogenet. 1996. PMID: 8956864

8

Monoallelic p53 deletion in chronic lymphocytic leukemia detected by interphase cytogenetics.

Amiel A, Arbov L, Manor Y, Fejgin M, Elis A, Gaber E, Lishner M. Amiel A, et al. Cancer Genet Cytogenet. 1997 Sep;97(2):97-100. doi: 10.1016/s0165-4608(96)00341-x. Cancer Genet Cytogenet. 1997. PMID: 9283589

9

Replication pattern in cancer: asynchronous replication in multiple myeloma and in monoclonal gammopathy.

Amiel A, Kirgner I, Gaber E, Manor Y, Fejgin M, Lishner M. Amiel A, et al. Cancer Genet Cytogenet. 1999 Jan 1;108(1):32-7. doi: 10.1016/s0165-4608(98)00107-1. Cancer Genet Cytogenet. 1999. PMID: 9973921

10

Deletion of 6q27 in chronic lymphocytic leukemia and multiple myeloma detected by fluorescence in situ hybridization.

Amiel A, Mulchanov I, Elis A, Gaber E, Manor Y, Fejgin M, Lishner M. Amiel A, et al. Cancer Genet Cytogenet. 1999 Jul 1;112(1):53-6. doi: 10.1016/s0165-4608(98)00255-6. Cancer Genet Cytogenet. 1999. PMID: 10432937

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