Rao KW - Search Results

1

Clonal karyotypic abnormalities associated with reactive lymphoid hyperplasia.

Montgomery ND, Mathews SP, Coward WB 4th, Rao KW, Fedoriw Y. Montgomery ND, et al. Among authors: rao kw. Cancer Genet. 2013 Apr;206(4):135-9. doi: 10.1016/j.cancergen.2013.03.003. Epub 2013 Apr 25. Cancer Genet. 2013. PMID: 23623181

2

Karyotypic abnormalities associated with Epstein-Barr virus status in classical Hodgkin lymphoma.

Montgomery ND, Coward WB 4th, Johnson S, Yuan J, Gulley ML, Mathews SP, Kaiser-Rogers K, Rao KW, Sanger WG, Sanmann JN, Fedoriw Y. Montgomery ND, et al. Among authors: rao kw. Cancer Genet. 2016 Sep;209(9):408-416. doi: 10.1016/j.cancergen.2016.08.006. Epub 2016 Aug 15. Cancer Genet. 2016. PMID: 27751359

3

Masked hypodiploidy: Hypodiploid acute lymphoblastic leukemia (ALL) mimicking hyperdiploid ALL in children: A report from the Children's Oncology Group.

Carroll AJ, Shago M, Mikhail FM, Raimondi SC, Hirsch BA, Loh ML, Raetz EA, Borowitz MJ, Wood BL, Maloney KW, Mattano LA Jr, Larsen EC, Gastier-Foster J, Stonerock E, Ell D, Kahwash S, Devidas M, Harvey RC, Chen IL, Willman CL, Hunger SP, Winick NJ, Carroll WL, Rao KW, Heerema NA. Carroll AJ, et al. Among authors: rao kw. Cancer Genet. 2019 Oct;238:62-68. doi: 10.1016/j.cancergen.2019.07.009. Epub 2019 Jul 30. Cancer Genet. 2019. PMID: 31425927 Free PMC article.

4

Holoprosencephaly in an infant with a minute deletion of chromosome 21(q22.3).

Estabrooks LL, Rao KW, Donahue RP, Aylsworth AS. Estabrooks LL, et al. Among authors: rao kw. Am J Med Genet. 1990 Jul;36(3):306-9. doi: 10.1002/ajmg.1320360312. Am J Med Genet. 1990. PMID: 2363428

5

Submicroscopic deletion 9(q34.3) and duplication 19(p13.3): identified by subtelomere specific FISH probes.

Quigley DI, Kaiser-Rogers K, Aylsworth AS, Rao KW. Quigley DI, et al. Among authors: rao kw. Am J Med Genet A. 2004 Feb 15;125A(1):67-72. doi: 10.1002/ajmg.a.20457. Am J Med Genet A. 2004. PMID: 14755469 Review.

6

Fragile X phenotype in a patient with a large de novo deletion in Xq27-q28.

Albright SG, Lachiewicz AM, Tarleton JC, Rao KW, Schwartz CE, Richie R, Tennison MB, Aylsworth AS. Albright SG, et al. Among authors: rao kw. Am J Med Genet. 1994 Jul 15;51(4):294-7. doi: 10.1002/ajmg.1320510403. Am J Med Genet. 1994. PMID: 7942990

7

Multiple congenital malformations in an infant prenatally diagnosed with mosaicism for dup(lq) and del(Xq).

Wells SR, Kuller JA, Rao KW, Aylsworth AS. Wells SR, et al. Among authors: rao kw. Clin Genet. 1996 Apr;49(4):216-9. doi: 10.1111/j.1399-0004.1996.tb03290.x. Clin Genet. 1996. PMID: 8828989 Review.

8

Usefulness and limitations of FISH to characterize partially cryptic complex chromosome rearrangements.

Kaiser-Rogers KA, Rao KW, Michaelis RC, Lese CM, Powell CM. Kaiser-Rogers KA, et al. Among authors: rao kw. Am J Med Genet. 2000 Nov 6;95(1):28-35. doi: 10.1002/1096-8628(20001106)95:1<28::aid-ajmg7>3.0.co;2-c. Am J Med Genet. 2000. PMID: 11074491

9

Section E6.1-6.4 of the ACMG technical standards and guidelines: chromosome studies of neoplastic blood and bone marrow-acquired chromosomal abnormalities.

Mikhail FM, Heerema NA, Rao KW, Burnside RD, Cherry AM, Cooley LD. Mikhail FM, et al. Among authors: rao kw. Genet Med. 2016 Jun;18(6):635-42. doi: 10.1038/gim.2016.50. Epub 2016 Apr 28. Genet Med. 2016. PMID: 27124785 Free article.

10

Section E6.5 of the ACMG technical standards and guidelines: chromosome studies for solid tumor abnormalities.

Cooley LD, Mascarello JT, Hirsch B, Jacky PB, Rao PN, Saxe D, Rao KW; Working Group of the American College of Medical Genetics (ACMG) Laboratory Quality Assurance Committee. Cooley LD, et al. Among authors: rao pn, rao kw. Genet Med. 2009 Dec;11(12):890-7. doi: 10.1097/GIM.0b013e3181bb7808. Genet Med. 2009. PMID: 20010366 Free article.

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