Velagaleti GV - Search Results

1

Fine mapping of breakpoints in two unrelated patients with rare overlapping interstitial deletions of 9q with mild dysmorphic features.

Kulharya AS, Flannery DB, Norris K, Lovell C, Levy B, Velagaleti GV. Kulharya AS, et al. Among authors: velagaleti gv. Am J Med Genet A. 2008 Sep 1;146A(17):2234-41. doi: 10.1002/ajmg.a.32397. Am J Med Genet A. 2008. PMID: 18666229

2

Unique case of mosaicism involving two morphologically similar marker chromosomes of different centric origin in a patient with developmental delay.

Levy B, Jalal SM, Dunn TM, Warburton PE, Tonk VS, Hirschhorn K, Lockhart LH, Hughes T, Velagaleti GV. Levy B, et al. Among authors: velagaleti gv. Am J Med Genet. 2002 Mar 15;108(3):198-204. doi: 10.1002/ajmg.10263. Am J Med Genet. 2002. PMID: 11891685

3

Molecular cytogenetic characterization of a unique and complex de novo 8p rearrangement.

Cooke SL, Northup JK, Champaige NL, Zinser W, Edwards PA, Lockhart LH, Velagaleti GV. Cooke SL, et al. Among authors: velagaleti gv. Am J Med Genet A. 2008 May 1;146A(9):1166-72. doi: 10.1002/ajmg.a.32248. Am J Med Genet A. 2008. PMID: 18302246

4

First report of an interstitial deletion, del(5)(q33.1q35.1) in a girl with primary amenorrhea, seizures, and severe behavioral and developmental deficiencies.

Northup JK, Wain KE, Hawkins JC, Matalon R, Velagaleti GV. Northup JK, et al. Among authors: velagaleti gv. Am J Med Genet A. 2008 Oct 1;146A(19):2578-82. doi: 10.1002/ajmg.a.32486. Am J Med Genet A. 2008. PMID: 18792973 No abstract available.

5

Position effects due to chromosome breakpoints that map approximately 900 Kb upstream and approximately 1.3 Mb downstream of SOX9 in two patients with campomelic dysplasia.

Velagaleti GV, Bien-Willner GA, Northup JK, Lockhart LH, Hawkins JC, Jalal SM, Withers M, Lupski JR, Stankiewicz P. Velagaleti GV, et al. Am J Hum Genet. 2005 Apr;76(4):652-62. doi: 10.1086/429252. Epub 2005 Feb 22. Am J Hum Genet. 2005. PMID: 15726498 Free PMC article.

6

A complex chromosome rearrangement, der(6)ins(6)(p21.1q25.3q27)inv(6)(p25.3q27), in a child with cleidocranial dysplasia.

Northup JK, Matalon R, Lockhart LH, Hawkins JC, Velagaleti GV. Northup JK, et al. Among authors: velagaleti gv. Eur J Med Genet. 2011 Jul-Aug;54(4):e394-8. doi: 10.1016/j.ejmg.2011.03.011. Epub 2011 Apr 3. Eur J Med Genet. 2011. PMID: 21466863

7

Most Jacobsen syndrome deletion breakpoints occur distal to FRA11B.

Michaelis RC, Velagaleti GV, Jones C, Pivnick EK, Phelan MC, Boyd E, Tarleton J, Wilroy RS, Tunnacliffe A, Tharapel AT. Michaelis RC, et al. Among authors: velagaleti gv. Am J Med Genet. 1998 Mar 19;76(3):222-8. Am J Med Genet. 1998. PMID: 9508241

8

Interstitial deletion of 20q in a patient with Waldenström macroglobulinemia following chemotherapy.

Blann MM, Velagaleti GV, Morgan DL, Martinez RE, Conlin PA, Tonk VS. Blann MM, et al. Among authors: velagaleti gv. Cancer Genet Cytogenet. 2002 Jan 15;132(2):145-8. doi: 10.1016/s0165-4608(01)00538-6. Cancer Genet Cytogenet. 2002. PMID: 11850077

9

Partial hexasomy for the Prader-Willi-Angelman syndrome critical region due to a maternally inherited large supernumerary marker chromosome.

Hoppman-Chaney NL, Dawson DB, Nguyen L, Sengupta S, Reynolds K, McPherson E, Velagaleti G. Hoppman-Chaney NL, et al. Am J Med Genet A. 2010 Aug;152A(8):2034-8. doi: 10.1002/ajmg.a.33483. Am J Med Genet A. 2010. PMID: 20602489

10

Familial interstitial deletion of chromosome 4 (p15.2p16.1).

Tonk VS, Jalal SM, Gonzalez J, Kennedy A, Velagaleti GV. Tonk VS, et al. Among authors: velagaleti gv. Ann Genet. 2003 Oct-Dec;46(4):453-8. doi: 10.1016/s0003-3995(03)00029-7. Ann Genet. 2003. PMID: 14659781

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