Mulvihill JJ - Search Results

1

Leiomyosarcoma of the breast: a pathologic and comparative genomic hybridization study of two cases.

Lee J, Li S, Torbenson M, Liu QZ, Lind S, Mulvihill JJ, Bane B, Wang J. Lee J, et al. Among authors: mulvihill jj. Cancer Genet Cytogenet. 2004 Feb;149(1):53-7. doi: 10.1016/S0165-4608(03)00286-3. Cancer Genet Cytogenet. 2004. PMID: 15104283

2

A variant t(8;10;21) in a patient with pathological features mimicking atypical chronic myeloid leukemia.

Lee J, Kern WF, Cain JB, Mulvihill JJ, Li S. Lee J, et al. Among authors: mulvihill jj. Cancer Genet Cytogenet. 2005 May;159(1):79-83. doi: 10.1016/j.cancergencyto.2004.10.002. Cancer Genet Cytogenet. 2005. PMID: 15860363

3

Cytogenetic and molecular cytogenetic studies of a variant of t(21;22), ins(22;21)(q12;q21q22), with a deletion of the 3' EWSR1 gene in a patient with Ewing sarcoma.

Lee J, Hopcus-Niccum DJ, Mulvihill JJ, Li S. Lee J, et al. Among authors: mulvihill jj. Cancer Genet Cytogenet. 2005 Jun;159(2):177-80. doi: 10.1016/j.cancergencyto.2004.11.003. Cancer Genet Cytogenet. 2005. PMID: 15899394

4

A novel subtelomeric translocation t(5;9) and a deletion of the RB1 gene in a patient with acute myeloid leukemia (AML-M0).

Lee J, Lu X, Shin ES, Kern WF, Mulvihill JJ, Li S. Lee J, et al. Among authors: mulvihill jj. Cancer Genet Cytogenet. 2008 Feb;181(1):36-9. doi: 10.1016/j.cancergencyto.2007.10.012. Cancer Genet Cytogenet. 2008. PMID: 18262051

5

Deletion of 14q24.1 approximately q24.3 in a patient with acute lymphoblastic leukemia: a hidden chromosomal anomaly detected by array-based comparative genomic hybridization.

Xu W, Lu X, Kim Y, Luo Y, Martin M, Mulvihill JJ, Li S. Xu W, et al. Among authors: mulvihill jj. Cancer Genet Cytogenet. 2008 Aug;185(1):43-6. doi: 10.1016/j.cancergencyto.2008.04.007. Cancer Genet Cytogenet. 2008. PMID: 18656693

6

A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome.

Hassed SJ, Hopcus-Niccum D, Zhang L, Li S, Mulvihill JJ. Hassed SJ, et al. Among authors: mulvihill jj. Clin Genet. 2004 May;65(5):400-4. doi: 10.1111/j.0009-9163.2004.0212.x. Clin Genet. 2004. PMID: 15099348

7

Down syndrome with pure partial trisomy 21q22 due to a paternal insertion (4;21) uncovered by uncultured amniotic fluid interphase FISH.

Lee J, Stanley JR, Vaz SA, Mulvihill JJ, Wilson P, Hopcus-Niccum D, Li S. Lee J, et al. Among authors: mulvihill jj. Am J Med Genet A. 2005 Jan 15;132A(2):206-8. doi: 10.1002/ajmg.a.30449. Am J Med Genet A. 2005. PMID: 15578618

8

Duplication 15q in a patient with t(8;21) acute myeloblastic leukemia (M2).

Zhang L, Mulvihill JJ, Kinasewitz GT, Scott KV, Bates F, Li S. Zhang L, et al. Among authors: mulvihill jj. Cancer Genet Cytogenet. 2002 Mar;133(2):148-51. doi: 10.1016/s0165-4608(01)00596-9. Cancer Genet Cytogenet. 2002. PMID: 11943342

9

Duplication 15q as the sole anomaly in an acute promyelocytic leukemia patient without t(15;17).

Zhang L, Mulvihill JJ, Kern WF, McMinn J, Li S. Zhang L, et al. Among authors: mulvihill jj. Cancer Genet Cytogenet. 2002 Oct 1;138(1):17-21. doi: 10.1016/s0165-4608(02)00538-1. Cancer Genet Cytogenet. 2002. PMID: 12419579

10

Identification of t(15;17) and a segmental duplication of chromosome 11q23 in a patient with acute myeloblastic leukemia M2.

Li S, Zhang L, Kern WF, Andrade D, Forsberg JE, Bates FR, Mulvihill JJ. Li S, et al. Among authors: mulvihill jj. Cancer Genet Cytogenet. 2002 Oct 15;138(2):149-52. doi: 10.1016/s0165-4608(02)00588-5. Cancer Genet Cytogenet. 2002. PMID: 12505261

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