Velagaleti GV - Search Results

1

Infant with midline thoracoabdominal schisis and limb defects.

Pivnick EK, Kaufman RA, Velagaleti GV, Gunther WM, Abramovici D. Pivnick EK, et al. Among authors: velagaleti gv. Teratology. 1998 Nov;58(5):205-8. doi: 10.1002/(SICI)1096-9926(199811)58:5<205::AID-TERA7>3.0.CO;2-X. Teratology. 1998. PMID: 9839359

2

Jacobsen syndrome: report of a patient with severe eye anomalies, growth hormone deficiency, and hypothyroidism associated with deletion 11 (q23q25) and review of 52 cases.

Pivnick EK, Velagaleti GV, Wilroy RS, Smith ME, Rose SR, Tipton RE, Tharapel AT. Pivnick EK, et al. Among authors: velagaleti gv. J Med Genet. 1996 Sep;33(9):772-8. doi: 10.1136/jmg.33.9.772. J Med Genet. 1996. PMID: 8880580 Free PMC article. Review.

3

Simultaneous adrenocortical carcinoma and ganglioneuroblastoma in a child with Turner syndrome and germline p53 mutation.

Pivnick EK, Furman WL, Velagaleti GV, Jenkins JJ, Chase NA, Ribeiro RC. Pivnick EK, et al. Among authors: velagaleti gv. J Med Genet. 1998 Apr;35(4):328-32. doi: 10.1136/jmg.35.4.328. J Med Genet. 1998. PMID: 9598730 Free PMC article.

4

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

5

Rapid identification of marker chromosomes using primed in situ labeling (PRINS).

Velagaleti GV, Tharapel SA, Martens PR, Tharapel AT. Velagaleti GV, et al. Am J Med Genet. 1997 Aug 8;71(2):130-3. doi: 10.1002/(sici)1096-8628(19970808)71:2<130::aid-ajmg2>3.0.co;2-1. Am J Med Genet. 1997. PMID: 9217209

6

Chromosome duplications and deletions and their mechanisms of origin.

Tharapel AT, Michaelis RC, Velagaleti GV, Laundon CH, Martens PR, Buchanan PD, Teague KE, Tharapel SA, Wilroy RS Jr. Tharapel AT, et al. Among authors: velagaleti gv. Cytogenet Cell Genet. 1999;85(3-4):285-90. doi: 10.1159/000015314. Cytogenet Cell Genet. 1999. PMID: 10449919

7

Validation of primed in situ labeling (PRINS) for interphase analysis: comparative studies with conventional fluorescence in situ hybridization and chromosome analyses.

Velagaleti GV, Tharapel SA, Tharapel AT. Velagaleti GV, et al. Cancer Genet Cytogenet. 1999 Jan 15;108(2):100-6. doi: 10.1016/s0165-4608(98)00124-1. Cancer Genet Cytogenet. 1999. PMID: 9973935

8

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

9

Down syndrome with biparental inheritance of der(14q21q) and maternally derived trisomy 21: confirmation by fluorescent in situ hybridization and microsatellite polymorphism analysis.

Rajangam S, Michaelis RC, Velagaleti GV, Lincoln S, Hegde S, Lewin S, Tarleton J, Thomas IM, Tharapel AT. Rajangam S, et al. Among authors: velagaleti gv. Am J Med Genet. 1997 May 2;70(1):43-7. doi: 10.1002/(sici)1096-8628(19970502)70:1<43::aid-ajmg9>3.0.co;2-s. Am J Med Genet. 1997. PMID: 9129740

10

Clinical applications of primed in situ labelling (PRINS) rapid identification of a marker chromosome in a fetus.

Velagaleti GV, Carpenter NJ, Tharapel AT. Velagaleti GV, et al. Ann Genet. 1997;40(3):154-7. Ann Genet. 1997. PMID: 9401104

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