Li S - Search Results

1

16p13.3 duplication associated with non-syndromic pierre robin sequence with incomplete penetrance.

Sun M, Zhang H, Li G, Wang X, Lu X, Sternenberger A, Guy C, Li W, Lee J, Zheng L, Li S. Sun M, et al. Among authors: li s, li g, li w. Mol Cytogenet. 2014 Nov 25;7(1):76. doi: 10.1186/s13039-014-0076-5. eCollection 2014. Mol Cytogenet. 2014. PMID: 25493098 Free PMC article.

2

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: li s. Cancer Genet Cytogenet. 2002 Mar;133(2):148-51. doi: 10.1016/s0165-4608(01)00596-9. Cancer Genet Cytogenet. 2002. PMID: 11943342

3

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: li s. Cancer Genet Cytogenet. 2004 Feb;149(1):53-7. doi: 10.1016/S0165-4608(03)00286-3. Cancer Genet Cytogenet. 2004. PMID: 15104283

4

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: li s. 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

5

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: li s. Cancer Genet Cytogenet. 2005 May;159(1):79-83. doi: 10.1016/j.cancergencyto.2004.10.002. Cancer Genet Cytogenet. 2005. PMID: 15860363

6

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: li s. Cancer Genet Cytogenet. 2005 Jun;159(2):177-80. doi: 10.1016/j.cancergencyto.2004.11.003. Cancer Genet Cytogenet. 2005. PMID: 15899394

7

Ring chromosome 9 [r(9)(p24q34)]: a report of two cases.

Purandare SM, Lee J, Hassed S, Steele MI, Blackett PR, Mulvihill JJ, Li S. Purandare SM, et al. Among authors: li s. Am J Med Genet A. 2005 Oct 15;138A(3):229-35. doi: 10.1002/ajmg.a.30382. Am J Med Genet A. 2005. PMID: 16158426

8

Trisomy 1q in a patient with severe aplastic anemia.

Angelidis P, Kojouri K, Lee J, Kern W, Mulvihill JJ, Li S. Angelidis P, et al. Among authors: li s. Cancer Genet Cytogenet. 2006 Aug;169(1):73-5. doi: 10.1016/j.cancergencyto.2006.03.014. Cancer Genet Cytogenet. 2006. PMID: 16875941

9

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: li s. Cancer Genet Cytogenet. 2008 Feb;181(1):36-9. doi: 10.1016/j.cancergencyto.2007.10.012. Cancer Genet Cytogenet. 2008. PMID: 18262051

10

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: li s. Cancer Genet Cytogenet. 2008 Aug;185(1):43-6. doi: 10.1016/j.cancergencyto.2008.04.007. Cancer Genet Cytogenet. 2008. PMID: 18656693

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