Velagaleti GV - Search Results

1

Molecular cytogenetic characterization of a familial der(1)del(1)(p36.33)dup(1)(p36.33p36.22) with variable phenotype.

Tonk VS, Wilson GN, Yatsenko SA, Stankiewicz P, Lupski JR, Schutt RC, Northup JK, Velagaleti GV. Tonk VS, et al. Among authors: velagaleti gv. Am J Med Genet A. 2005 Dec 1;139A(2):136-40. doi: 10.1002/ajmg.a.30958. Am J Med Genet A. 2005. PMID: 16278888

2

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

3

Molecular cytogenetic characterization of a recombinant chromosome rec(22)dup(22q)inv(22)(p13q12.2).

Tonk VS, Jesurun CA, Morgan DL, Lockhart LH, Velagaleti GV. Tonk VS, et al. Among authors: velagaleti gv. Am J Med Genet A. 2004 Jan 1;124A(1):92-5. doi: 10.1002/ajmg.a.20384. Am J Med Genet A. 2004. PMID: 14679594

4

Molecular cytogenetic characterization of an interstitial de novo 13q deletion in a 3-month-old with severe pediatric gastroesophageal reflux.

Champaigne NL, Laird NA, Northup JK, Velagaleti GV. Champaigne NL, et al. Among authors: velagaleti gv. Am J Med Genet A. 2009 Feb 15;149A(4):751-4. doi: 10.1002/ajmg.a.32733. Am J Med Genet A. 2009. PMID: 19291769

5

Duplication 8 [inv dup(8)(p12p23)] with macrocephaly.

Tonk VS, Wilson GN, Velagaleti GV. Tonk VS, et al. Among authors: velagaleti gv. Ann Genet. 2001 Oct-Dec;44(4):195-9. doi: 10.1016/s0003-3995(01)01089-9. Ann Genet. 2001. PMID: 11755105

6

Complex/variant translocations in chronic myelogenous leukemia (CML): genesis and prognosis with 4 new cases.

Mendiola C, Ortega V, Tonk VS, Coviello JM, Velagaleti G. Mendiola C, et al. Exp Mol Pathol. 2014 Aug;97(1):105-10. doi: 10.1016/j.yexmp.2014.06.004. Epub 2014 Jun 11. Exp Mol Pathol. 2014. PMID: 24927873

7

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

8

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.

9

Interphase FISH screening for the LCR-mediated common rearrangement of isochromosome 17q in primary myelofibrosis.

Bien-Willner GA, Stankiewicz P, Lupski JR, Northup JK, Velagaleti GV. Bien-Willner GA, et al. Among authors: velagaleti gv. Am J Hematol. 2005 Aug;79(4):309-13. doi: 10.1002/ajh.20366. Am J Hematol. 2005. PMID: 16044457 Free article.

10

Subtelomeric rearrangements in idiopathic mental retardation.

Velagaleti GV, Robinson SS, Rouse BM, Tonk VS, Lockhart LH. Velagaleti GV, et al. Indian J Pediatr. 2005 Aug;72(8):679-85. doi: 10.1007/BF02724077. Indian J Pediatr. 2005. PMID: 16131774

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

83 results

Search Page

Filters