Reddy KS - Search Results

1

Interstitial deletion of chromosome 4, del(4)(q12q21.1), in a mentally retarded boy with a piebald trait, due to maternal insertion, ins(8;4).

Fujimoto A, Reddy KS, Spinks R. Fujimoto A, et al. Among authors: reddy ks. Am J Med Genet. 1998 Jan 6;75(1):78-81. doi: 10.1002/(sici)1096-8628(19980106)75:1<78::aid-ajmg16>3.0.co;2-p. Am J Med Genet. 1998. PMID: 9450862 Review.

2

Subtle overlapping deletions in the terminal region of chromosome 6q24.2-q26: three cases studied using FISH.

Sukumar S, Wang S, Hoang K, Vanchiere CM, England K, Fick R, Pagon B, Reddy KS. Sukumar S, et al. Among authors: reddy ks. Am J Med Genet. 1999 Nov 5;87(1):17-22. Am J Med Genet. 1999. PMID: 10528241 Review.

3

Variants of chromosome 9 with additional euchromatic bands: two case reports.

Reddy KS. Reddy KS. Am J Med Genet. 1996 Sep 6;64(4):536-8. doi: 10.1002/(SICI)1096-8628(19960906)64:4<536::AID-AJMG2>3.0.CO;2-N. Am J Med Genet. 1996. PMID: 8870918

4

Two sibs with Wolf-Hirschhorn and DiGeorge deletions resulting from an unbalanced chromosome rearrangement, 45,XX/XY, der(4)t(4;22) (p16.3;q11.2) mat,-22.

Reddy KS, Sulcova V, Siassi B. Reddy KS, et al. J Med Genet. 1996 Oct;33(10):852-5. doi: 10.1136/jmg.33.10.852. J Med Genet. 1996. PMID: 8933340 Free PMC article.

5

De novo mosaic add(3) characterized to be trisomy 14q31-qter using spectral karyotyping and subtelomeric probes.

Reddy KS, Sulcova V, Young H, Blancato JK, Haddad BR. Reddy KS, et al. Am J Med Genet. 1999 Feb 12;82(4):318-21. doi: 10.1002/(sici)1096-8628(19990212)82:4<318::aid-ajmg8>3.0.co;2-0. Am J Med Genet. 1999. PMID: 10051165

6

Submicroscopic terminal deletion of 1p36.3 and Xp23 hidden in complex chromosome rearrangements: independent mechanism of telomere restitution on the two chromatids.

Reddy KS, Yang X. Reddy KS, et al. Am J Med Genet A. 2003 Mar 15;117A(3):261-7. doi: 10.1002/ajmg.a.10108. Am J Med Genet A. 2003. PMID: 12599190 Review.

7

Microdeletion of chromosome sub-band 2q37.3 in two patients with abnormal situs viscerum.

Reddy KS, Flannery D, Farrer RJ. Reddy KS, et al. Am J Med Genet. 1999 Jun 11;84(5):460-8. doi: 10.1002/(sici)1096-8628(19990611)84:5<460::aid-ajmg10>3.0.co;2-l. Am J Med Genet. 1999. PMID: 10360400 Review.

8

Mosaic tetrasomy 8q: inverted duplication of 8q23.3qter in an analphoid marker.

Reddy KS, Sulcova V, Schwartz S, Noble JE, Phillips J, Brasel JA, Huff K, Lin HJ. Reddy KS, et al. Am J Med Genet. 2000 May 1;92(1):69-76. Am J Med Genet. 2000. PMID: 10797426

9

A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity.

Reddy KS, Aradhya S, Meck J, Tiller G, Abboy S, Bass H. Reddy KS, et al. Genet Med. 2013 Jan;15(1):3-13. doi: 10.1038/gim.2012.78. Epub 2012 Aug 30. Genet Med. 2013. PMID: 22935720 Free article. Review.

10

SKY assessment of two karyotypes with 0-6 supernumerary marker/ring chromosomes and review of previously reported cases with two or more markers.

Reddy KS, Wang S, Groh S, Gonatos J. Reddy KS, et al. Am J Med Genet A. 2003 Apr 15;118A(2):156-71. doi: 10.1002/ajmg.a.10045. Am J Med Genet A. 2003. PMID: 12655496 Review.

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