K. S. Reddy

发表

Fluorescence in situ hybridization identifies inversion 16 masked by t(10;16)(q24;q22), t(7;16)(q21;q22), and t(2;16)(q37;q22) in three cases of AML-M4Eo.

K. S. Reddy, S. Wang, P. Montgomery, 2000, Cancer genetics and cytogenetics.

Oligoarray (105K) CGH Analysis of Chromosome Microdeletions within 10q22.1q24.32

R. Mardach, K. S. Reddy, H. Bass, 2010, Cytogenetic and Genome Research.

Intrachromosomal triplication of 2q11.2-q21 in a severely malformed infant: case report and review of triplications and their possible mechanism.

R. Lachman, K. S. Reddy, H. J. Lin, 1999, American journal of medical genetics.

Trisomy 15 in hematological disorders.

K. S. Reddy, A. Sbeiti, K. Reddy, 2000, Cancer genetics and cytogenetics.

A FISH study of variant Philadelphia rearrangements.

K. S. Reddy, V. Sulcova, K. Reddy, 2000, Cancer genetics and cytogenetics.

A child with ALL and ETV6/AML1 fusion on a chromosome 12 due to an insertion of AML1 and loss of ETV6 from the homolog involved in a t(12;15)(p13;q15)

K. S. Reddy, S. Wang, X. Yang, 2000, Genes, chromosomes & cancer.

FISH analysis of an AML-M5a with segmental rearrangements involving 11q23-MLL region.

T. L. Yu., K. S. Reddy, S. Wang, 2000, Cancer genetics and cytogenetics.

Segmental amplification of 11q23 region identified by fluorescence in situ hybridization in four patients with myeloid disorders: a review.

T. Saphner, M. Crow, K. S. Reddy, 2001, Cancer genetics and cytogenetics.

A paternally inherited terminal deletion, del(8)(p23.1)pat, detected prenatally in an amniotic fluid sample: a review of deletion 8p23.1 cases

K. S. Reddy, K. S. Reddy, 1999, Prenatal diagnosis.

Trisomy 14 and leukemia.

K. S. Reddy, K. Reddy, 1998, Cancer genetics and cytogenetics.

A half cryptic derivative der(18)t(5;18)pat identified by M‐FISH and subtelomere probes: clinical findings and review of subtelomeric rearrangements

K. S. Reddy, J. Fugate, K. Reddy, 1999, Clinical genetics.

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).

R. Spinks, A. Fujimoto, K. S. Reddy, 1998, American journal of medical genetics.

Effect of Cigarette Smoking on Male Fertility : A Prospective Hospital Based Study

K. S. Reddy, K. Reddy, 2018 .

Pathogenetics of 45,X/46,XY gonadal mosaicism

K. S. Reddy, V. Sulcova, 1998, Cytogenetic and Genome Research.

On the localization of mitomycin C-induced aberrations in normal human and Fanconi's anaemia cells.

J. Savage, K. S. Reddy, 1987, Mutation research.

An infant with a mosaic 45,X/46,X,psu dic(Y) (pter-->q11.2::q11.2-->pter) karyotype and mixed gonadal dysgenesis studied for extent of mosaicism in the gonads.

K. S. Reddy, C. Ho, V. Sulcova, 1996, American journal of medical genetics.

Triple aneuploidy in spontaneous abortions

K. S. Reddy, K. Reddy, 1999, Clinical genetics.

Jumping translocations involving chromosome 1q in a patient with Crohn disease and acute monocytic leukemia: a review of the literature on jumping translocations in hematological malignancies and Crohn disease.

K. S. Reddy, L. Parsons, L. Colman, 1999, Cancer genetics and cytogenetics.

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

K. S. Reddy, Shirong R Wang, S. Groh, 2003, American journal of medical genetics. Part A.

Double minutes (dmin) and homogeneously staining regions (hsr) in myeloid disorders: a new case suggesting that dmin form hsr in vivo

K. S. Reddy, K. Reddy, 2007, Cytogenetic and Genome Research.

A Philadelphia-negative chronic myeloid leukemia with a BCR/ABL fusion gene on chromosome 9.

K. S. Reddy, B. Grove, K. Reddy, 1998, Cancer genetics and cytogenetics.

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

D. Flannery, K. S. Reddy, R. Farrer, 1999, American journal of medical genetics.

Fusion of 9 beta-satellite and telomere (TTAGGG)n sequences results in a jumping translocation

K. S. Reddy, T. Murphy, 2000, Human Genetics.

Intrachromosomal triplications: molecular cytogenetic and clinical studies

K. S. Reddy, James J. Logan, K. Reddy, 2000, Clinical genetics.

Double trisomy in spontaneous abortions

K. S. Reddy, K. Reddy, 1997, Human Genetics.

An hsr on chromosome 7 was shown to be an insertion of four copies of the 11q23 MLL gene region in an HIV-related lymphoma.

K. S. Reddy, J. A. Chan, L. Mak, 2001, Cancer genetics and cytogenetics.

A molecular, cytogenetic, and clinical evaluation of mosaic tandem duplication 17p and Charcot-Marie-Tooth type 1A neuropathy.

K. S. Reddy, M. Larsen, K. Reddy, 1998, Journal of medical genetics.

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

R. Fick, K. S. Reddy, S. Wang, 1999, American journal of medical genetics.

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

S. Schwartz, J. Brasel, K. Reddy, 2000, American journal of medical genetics.

The mobile nature of acrocentric elements illustrated by three unusual chromosome variants

K. S. Reddy, V. Sulcova, K. Reddy, 1998, Human Genetics.

Replication kinetics of X chromosomes in fibroblasts and lymphocytes

D. Papworth, J. Savage, K. S. Reddy, 1988, Human Genetics.

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.

B. Siassi, K. S. Reddy, V. Sulcova, 1996, Journal of medical genetics.

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

K. S. Reddy, 1996, American journal of medical genetics.

Translocation (9;10) Pat, in a Male Child Leading to Monosomy 9p13→9pter and Trisomy 10q24→10qter

K. S. Reddy, S. Rajangam, I. M. Thomas, 2001 .