Velagaleti GV - Search Results

1

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

2

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.

3

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

4

Unusual pseudo dicentric, psu dic (1;19)(q10;q13.42), in a female with premature ovarian failure.

Northup J, Griffis K, Hawkins J, Lockhart L, Velagaleti G. Northup J, et al. Fertil Steril. 2007 Mar;87(3):697.e5-8. doi: 10.1016/j.fertnstert.2006.05.089. Epub 2006 Nov 29. Fertil Steril. 2007. PMID: 17140574 Free article.

5

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

6

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

7

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.

8

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

9

Do cytogenetic abnormalities precede morphologic abnormalities in a developing malignant condition?

Northup JK, Gadre SA, Ge Y, Lockhart LH, Velagaleti GV. Northup JK, et al. Among authors: velagaleti gv. Eur J Haematol. 2007 Feb;78(2):152-6. doi: 10.1111/j.1600-0609.2006.00798.x. Eur J Haematol. 2007. PMID: 17313561

10

Partial trisomy and partial monosomy resulting from a reciprocal segregating in a large family.

Velagaleti GV, Hawkins JC, Panova NI, Lockhart LH. Velagaleti GV, et al. Indian J Pediatr. 2008 Sep;75(9):956-60. doi: 10.1007/s12098-008-0093-7. Indian J Pediatr. 2008. PMID: 18568304

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