V. Dev

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Quinacrine fluorescent karyotypes of human diploid and heteroploid cell lines.

D. Miller, O. Miller, P. Allderdice, 1971, Cytogenetics.

An infant with deletion of the distal long arm of chromosome 15 (q26.1----qter) and loss of insulin-like growth factor 1 receptor gene.

M. Chrétien, M. Butler, M. Mbikay, 1991, American journal of medical genetics.

5-azacytidine decreases the frequency of fragile X expression in peripheral lymphocyte culture.

C. Mixon, V. Dev, 1984, American journal of medical genetics.

Frequency of FLT3 – internal tandem duplication (ITD) gene mutations in various cytogenetic groups in acute myelogenous leukemia (AML): A report from Tamil Nadu, India

G. Gu, Neng Li, V. Dev, 2021 .

Familial X centromere variant resulting in false‐positive prenatal diagnosis of monosomy X by interphase FISH

K. Tsuchiya, M. Schueler, V. Dev, 2001, Prenatal diagnosis.

A new human cell line derived from a poorly differentiated endometrial adenocarcinoma.

D. Gal, J. C. Porter, J. Forney, 1982, Gynecologic oncology.

Identification of the mouse karyotype by quinacrine fluorescence, and tentative assignment of seven linkage groups.

D. Miller, J. Hutton, R. E. Kouri, 1971, Proceedings of the National Academy of Sciences of the United States of America.

A novel t(2;20)(q35;p12) in embryonal rhabdomyosarcoma.

J. Whitlock, R. Ho, Joyce E. Johnson, 2004, Cancer genetics and cytogenetics.

Clinical evaluation of a DNA probe assay for the Philadelphia (Ph1) translocation in chronic myelogenous leukemia.

R. Chaganti, M. Talpaz, L. Chan, 1988, Leukemia.

Idiotypic cross-reactivity of immunoglobulins expressed in Waldenström's macroglobulinemia, chronic lymphocytic leukemia, and mantle zone lymphocytes of secondary B-cell follicles.

T. Kipps, R. Kyle, G. Silverman, 1991, Blood.

Quinacrine fluorescent chromosome analysis of the Snell translocation in the mouse.

D. Miller, J. Hutton, R. E. Kouri, 1972, Genetics.

Partial translocation of NOR and its activity in a balanced carrier and in her cri-du-chat fetus

V. Dev, J. Byrne, Gloria Bunch, 1979, Human Genetics.

Regulation of rRNA gene expression in a human familial 14p+ marker chromosome

D. Warburton, W. R. Breg, O. Miller, 1978, Human Genetics.

Techniques for Chromosome Analysis

R. Tantravahi, V. Dev, 1982 .

Nucleolus organizer regions in diploid and heteroploid chinese hamster cell lines.

L. Weide, C. S. Rupert, V. Dev, 1981 .

Activity of both mouse and Chinese hamster ribosomal RNA genes in somatic cell hybrids.

L. Weide, C. S. Rupert, V. Dev, 1979, Experimental cell research.

Understanding the fragile X syndrome.

V. Dev, J. Mixon, 1984, The Alabama journal of medical sciences.

Fragile X syndrome: clinical, cytogenetic, biochemical and molecular features

V. Dev, J. Mixon, 1986, Indian journal of pediatrics.

Interphase Chromosome Profiling: A Method for Conventional Banded Chromosome Analysis Using Interphase Nuclei.

N. Rao, P. Koduru, D. V. Van Dyke, 2017, Archives of pathology & laboratory medicine.

Duplication 12q mosaicism in two unrelated patients with a similar syndrome.

U. Francke, J. M. Optiz, M. Harrod, 1980, American journal of medical genetics.

Fragile X expression is decreased by 5-azacytidine and S-adenosylhomocysteine.

V. Dev, J. Mixon, 1983, American journal of human genetics.

Human–mouse cell hybrid with human multiple Y chromosomes

M. Marcus, R. Tantravahi, Dorothy A. Miller, 1976, Nature.

A rapid and reliable chromosome analysis method for products of conception using interphase nuclei

G. Gu, P. Koduru, D. V. Van Dyke, 2018, Molecular genetics & genomic medicine.

Double isotype production by a neoplastic B cell line. II. Allelically excluded production of mu and gamma 1 heavy chains without CH gene rearrangement

J. Uhr, E. Vitetta, P. Tucker, 1986, The Journal of experimental medicine.

DOUBLE ISOTYPE PRODUCTION BY A NEOPLASTIC

J. Uhr, E. Vitetta, P. Tucker, 1986 .

ABL deletion without associated BCR-ABL in precursor B-cell acute lymphoblastic leukemia.

G. Gu, Mingya Liu, V. Dev, 2009, Leukemia research : a Forum for Studies on Leukemia and Normal Hemopoiesis.

Chorionic villus sampling: quality control--a continuous improvement model.

F. Boehm, G. Reed, S. Salyer, 1993, American journal of obstetrics and gynecology.

Assignment of four linkage groups to chromosomes in Mus musculus and a cytogenetic method for locating their centromeric ends.

D. Miller, J. Hutton, R. E. Kouri, 1971, Proceedings of the National Academy of Sciences of the United States of America.

Identification by quinacrine fluorescence of the chromosome carrying mouse linkage group I in the Cattanach translocation.

D. Miller, J. Hutton, R. E. Kouri, 1971, Genetics.

Abnormal centromere-chromatid apposition (ACCA) and Peters' anomaly.

W. Wertelecki, D. Superneau, V. Dev, 1985, Ophthalmic paediatrics and genetics.

Two patients with ring chromosome 15 syndrome.

M. Butler, A. Fogo, J. Phillips, 1988, American journal of medical genetics.

Identification of a ring chromosome as a ring 8 using fluorescent in situ hybridization (FISH) in a child with multiple congenital anomalies.

M. Butler, G. A. Allen, V. Dev, 1995, American journal of medical genetics.

A child with 45,X/46,X,del(Y)(q12) identified with a Y-specific probe.

J. Trill, J. Tischfield, P. McDonough, 1986, Fertility and sterility.

The quinacrine fluorescence karyotype of Mus musculus and demonstration of strain differences in secondary constrictions.

D. Miller, J. Hutton, R. E. Kouri, 1971, Cytogenetics.

CYTOLOGICAL DETECTION OF THE cZsH DELETION INVOLVING THE ALBINO ( c ) LOCUS ON CHROMOSOME 7 IN THE MOUSE 1

D. Miller, J. Miller, V. Dev, 2003 .

Assignment of linkage groups 8 and X to chromosomes in Mus musculus and identification of the centromeric end of linkage group I.

D. Miller, J. Hutton, R. E. Kouri, 1971, Cytogenetics.

Characterization of a novel human pre-B leukemia cell line.

R. G. Smith, W. Shannon, V. Dev, 1981, Journal of immunology.

Use of the BCR probe to demonstrate extramedullary recurrence of CGL with a T cell lymphoid phenotype following bone marrow transplantation.

J. Whitlock, M. Kinney, S. Wolff, 1988, Bone marrow transplantation.

Pallister-Killian syndrome detected by fluorescence in situ hybridization.

V. Dev, M. Bulter, 1995, American journal of medical genetics.

Diagnosis of trisomy 18 in monozygotic twins by cordocentesis.

J. Ulm, P. Jeanty, J. Phillips, 1989, American journal of obstetrics and gynecology.

Reactivation of silent rRNA genes by simian virus 40 in human-mouse hybrid cells.

R. Baserga, K. Soprano, C. Croce, 1979, Proceedings of the National Academy of Sciences of the United States of America.

The use of early simultaneous percutaneous umbilical blood sampling (PUBS) and amniocentesis for prenatal fragile X chromosome diagnosis.

J. Ulm, M. Butler, L. Shapiro, 1988, American journal of medical genetics.

Direct karyotyping of unstimulated newborn blood: a rapid diagnostic method for the clinical management of critically ill newborns.

S. A. Tharapel, V. Dev, 1997, American journal of medical genetics.

Tion of strain differences in secondary constrictions.

J. Hutton, R. E. Kouri, M. Grewal, 1971 .

Unusual translocations t(2;6) and t(?;22) in a child with acute myelocytic leukemia.

A. Carroll, V. Mankad, W. Crist, 1983, Cancer Genetics and Cytogenetics.