H. Dosik

发表

Human chromosome heteromorphisms in Americans Blacks: II. Higher incidence of pericentric inversions of secondary constriction regions (h).

R. Verma, J. Rodríguez, H. Dosik, 1981, American journal of medical genetics.

H-y antigen: expression in human subjects with the testicular feminization syndrome.

S. Wachtel, E. Dorus, M. New, 1977, Science.

Serologic detection of a y-linked gene in xx males and xx true hermaphrodites.

S. Wachtel, H. Thaler, W. R. Breg, 1976, The New England journal of medicine.

Evidence of a new chimeric bcr/c-abl mRNA in patients with chronic myelocytic leukemia and the Philadelphia chromosome.

N. Heisterkamp, J. Groffen, G. Grosveld, 1985, The New England journal of medicine.

Case report: adult T-cell leukemia/lymphoma associated with recurrent strongyloides hyperinfection.

E. Tschachler, K. Phelps, H. Dosik, 1991, The American journal of the medical sciences.

Leukemia in Fanconi's anemia: cytogenetic and tumor virus susceptibility studies.

K. Hirschhorn, G. Todaro, Stanley L. Lee, 1970, Blood.

Transfusion and alloimmunization in sickle cell disease. The Cooperative Study of Sickle Cell Disease.

O. Castro, P. Levy, W. Rosse, 1990, Blood.

Photosensitivity, abnormal porphyrin profile, and sideroblastic anemia.

S. Sassa, N. Soter, H. Lim, 1992, Journal of the American Academy of Dermatology.

Cytosine arabinoside with daunorubicin or adriamycin for therapy of acute myelocytic leukemia: a CALGB study.

N. Nissen, E. Henderson, R. Silver, 1982, Blood.

Chromosomal abnormalities in adult T-cell leukemia/lymphoma (ATL)

M. Macera, J. Abramson, R. Verma, 1987, Journal of Cancer Research and Clinical Oncology.

Influence of renal failure on myelosuppressive effects of melphalan: Cancer and Leukemia Group B experience.

T. Pajak, H. Dosik, S. Kochwa, 1982, Cancer treatment reports.

Cytosine arabinoside with daunorubicin or adriamycin for therapy of acute myelocytic leukemia: a CALGB study.

N. Nissen, R. Silver, P. Raich, 1982, Blood.

Heteromorphisms of the Philadelphia (Ph1) Chromosome in Patients with Chronic Myelogenous Leukaemia (CML). I. CLASSIFICATION AND CLINICAL SIGNIFICANCE

R. Verma, H. Dosik, 1980, British journal of haematology.

The quantitative analysis of constitutive heterochromatic regions of human chromosomes 1, 9, and 16 in relation to size and inversion heteromorphisms in East Indians

R. Verma, H. Dosik, J. Rodriguez, 1982, Experientia.

Human chromosomal heteromorphism in American blacks. V. Racial differences in size variation of the short arm of acrocentric chromosomes

R. Verma, H. Dosik, 1981, Experientia.

Unusual translocations involving chromosomes 12;22 and 9;12 in a case of chronic myelogenous leukemia.

R. Silver, R. Verma, M. Coleman, 1985, Cancer genetics and cytogenetics.

Human chromosomal heteromorphisms in american blacks

R. Verma, H. Dosik, Harvey Dosik, 1980, Human Genetics.

The first report of familial adult T‐cell leukemia lymphoma in the United States

J. Abramson, H. Dosik, J. Abramson, 1988, American journal of hematology.

Cytogenetic studies of blast cells in the cerebrospinal fluid in meningeal leukemia.

R. Verma, H. Dosik, J. Rodriguez, 1984, Cancer genetics and cytogenetics.

Acquired lipidosis: Gaucher-like cells and "blue cells" in chronic granulocytic leukemia.

F. Rosner, H. Dosik, A. Sawitsky, 1972, Seminars in hematology.

Chronic hepatitis C in patients with sickle cell disease.

G. Posner, R. Bellevue, H. Dosik, 1996, The American journal of gastroenterology.

Sv40 t‐antigen expression in skin fibroblasts from clinically normal individuals and from ten cases of fanconi anemia

W. Blattner, A. Lubiniecki, C. Sun, 1977, American journal of hematology.

Bullous eruption and elevated leukocyte alkaline phosphatase in the course of busulfan-treated chronic granulocytic leukemia.

F. Rosner, H. Dosik, D. Hurewitz, 1970, Blood.

Histiocytic lymphoma fifteen years following remission of acute lymphoblastic leukemia.

H. Dosik, S. L. Lee, R. Añón, 1980, Blood.

Chromosomal Abnormality in the Newborns of Hepatitis B Surface Antigen (HBsAg) Carrier Mothers

R. Verma, H. Evans, H. Dosik, 1980, Clinical pediatrics.

Cytogenetic polymorphism or Y/15 translocation in a black male with ambiguous genitalia.

R. Verma, H. Dosik, R. Jhaveri, 1978, Journal de genetique humaine.

Length heteromorphisms of fluorescent (f) and non-fluorescent (nf) segments of human Y chromosome: classification, frequencies, and incidence in normal Caucasians.

H. Lubs, R. Verma, H. Dosik, 1978, Journal of medical genetics.

Y-chromosomal genes in a phenotypic male with a 46XX karyotype.

G. Koo, H. Dosik, G. Spergel, 1976, JAMA.

An improved method for photographing fluorescent human chromosomes *

R. Verma, H. Dosik, 1976 .

A possible reason for clustering of trisomy 18 in humans

R. Verma, H. Evans, H. Dosik, 1980, Clinical genetics.

Anthramycin-induced sister-chromatid exchange and caffeine potentiation in the chromosomes of Indian muntjac.

R. Verma, H. Dosik, S. V. Ved Brat, 1979, Mutation research.

Expression of nucleolus organizer regions (NORs) in human acrocentric chromosomes by NSG, QFQ and RFA techniques: are they identical?

R. Verma, H. Dosik, C. Benjamin, 1983, Cytobios.

Gaucher cells in leukemia.

A. N. Morrison, F. Rosner, H. Dosik, 1969, JAMA.

Prevention of neonatal hepatitis B infection by high-dose hepatitis B immune globulin.

H. Dosik, R. Jhaveri, 1978, The New England journal of medicine.

High titer multiple dose therapy with HBIG in newborn infants of HBsAg positive mothers.

H. Evans, H. Dosik, R. Jhaveri, 1980, The Journal of pediatrics.

Transfusion and Alloimmunization in Sickle Cell Disease

Wendell, O. Castro, Winfred C. Wang, 2003 .

Transfusion and alloimmunization in sickle cell disease. The Cooperative Study of Sickle Cell Disease

O. Castro, Winfred C. Wang, P. Levy, 1990 .

Gaucher cells in leukemia.

F. Rosner, H. Dosik, 1970, The Journal of pediatrics.

Pseudohyperkalemia and leukocytosis.

H. Dosik, 1977, Blood.

Human chromosomal heteromorphisms: nature and clinical significance.

R. Verma, H. Dosik, 1980, International review of cytology.

Racial variation of a non-fluorescent segment of the Y chromosome in East Indians.

R. Verma, H. Dosik, A. Huq, 1983, Journal of medical genetics.

Chronic myelogenous leukemia presenting in the blastic phase and its association with a 45 XO Ph1 karyotype.

H. Dosik, R. Nigam, 1976, Blood.

Rapid identification of chromosomal abnormalities in human neoplasia.

R. Verma, A. Babu, H. Dosik, 1986, Stain technology.

Alpha Thalassaemia in American Blacks: a Study of a Family with Five Cases of Haemoglobin H Disease

R. Bellevue, R. Rieder, H. Dosik, 1979, British journal of haematology.

Long Survival in Philadelphia-Chromosome-Positive Acute Leukemia

R. Verma, H. Dosik, I. Sahdev, 1986, Tumori.

Relationship of SV40 T‐antigen expression in vitro to disorders of bone marrow function

W. Blattner, A. Lubiniecki, W. Blattner, 1980, American journal of hematology.

SV40 T‐Antigen Expression in Acute Non‐lymphocytic Leukaemia

A. Lubiniecki, W. Blattner, H. Dosik, 1979, British journal of haematology.

Population heteromorphisms of Ag-stained nucleolus organizer regions (NORs) in the acrocentric chromosomes of East Indians

R. Verma, H. Dosik, Jorge Rodríguez, 2004, Human Genetics.

Preferential association of nucleolar organizing human chromosomes as revealed by silver staining technique at mitosis

J. V. Shah, R. Verma, H. Dosik, 2004, Molecular and General Genetics MGG.

Frequency of RFA colour polymorphisms of human acrocentric chromosomes in Caucasians: interrelationship with QFQ polymorphisms

H. Lubs, R. Verma, H. Dosik, 1977, Annals of human genetics.

Severe persistent neutropenia, direct positive antiglobulin reaction and familial IgA deficiency.

F. Rosner, H. Dosik, A. Alter, 1972, Israel journal of medical sciences.

Double trisomy 48,XXX,+ 18 in a newborn.

R. Verma, H. Dosik, R. Jhaveri, 1981, American journal of medical genetics.

Partial duplication for the short arm of chromosome 2 : the 2p23 to pter syndrome.

R. Verma, H. Evans, H. Dosik, 1982, Annales de genetique.

Purulent Pericarditis in Acute Leukemia

H. Dosik, R. Jhaveri, L. Lavorgna, 1979, La Clinica pediatrica.

48,XXX, +18 double trisomy

H. Dosik, I. Wexler, D. P. Madahar, 1974 .

Higher Incidence of Small Y Chromosome in Humans with Trisomy 21 (Down Syndrome)

R. Verma, H. Dosik, Q. Qazi, 1982, Pediatric Research.

Case report bland cholestasis

H. Dosik, M. Krishnamurthy, A. Elguezabal, 1978 .

Bland cholestasis. Unusual hepatic sequela in sickle cell anemia.

H. Dosik, M. Krishnamurthy, A. Elguezabal, 1978, Postgraduate medicine.

Chromosome fragility in Bloom's syndrome cell line GM 1492.

R. Verma, H. Dosik, S. V. Ved Brat, 1984, Cancer genetics and cytogenetics.

Sister chromatid differentiation and isolabeling of chromosomes

R. Verma, H. Dosik, S. V. Ved Brat, 1981, Human Genetics.

Ring chromosome 13 in a child with minor dysmorphic features. Irregular phenotypic expression of ring 13 syndrome.

R. Verma, H. Dosik, R. Jhaveri, 1978, American journal of diseases of children.

Lymphosarcoma of the breast.

H. Dosik, A. Elguezabal, M. Ti, 1975, The American journal of the medical sciences.

Structural Organization of Heterochromatin in the Human Genome

R. Verma, H. Dosik, 1987 .

A simple technique for obtaining prometaphase chromosomes from lymphocytes.

J. V. Shah, R. Verma, J. Rodríguez, 1983, Journal of Medical Genetics.

Human chromosomes in prenatal diagnosis: A one step high resolution technique

J. V. Shah, R. Verma, H. Dosik, 1983, Prenatal diagnosis.

Short communication: no evidence of HTLV-3 and HTLV-4 infection in New York State subjects at risk for retroviral infection.

F. Siegal, C. Welch, Anish Thomas, 2010, AIDS research and human retroviruses.

Chronic Myelogenous Leukemia Presenting in the Blastic Phase and Its Association With a 45 XO Ph ’ Karyotype

H. Dosik, 2005 .

Thrombotic Thrombocytopenic Purpura in Patients with the Acquired Immunodeficiency Syndrome (AIDS)-Related Complex: A Report of Two Cases

R. Bellevue, H. Dosik, M. Bertoni, 1988 .

Pseudohyperkalemia and extreme leukocytosis.

R. Bellevue, H. Dosik, G. Spergel, 1975, The Journal of laboratory and clinical medicine.

Incidence of major chromosomal abnormalities in a referred population for suspected chromosomal aberrations: a report of 357 cases

R. Verma, H. Dosik, 1980, Clinical genetics.

Psychosocial aspects of sickle-cell anemia in adolescents.

H. Dosik, M. Krishnamurthy, S. Conyard, 1980, Health & social work.

Peripheral location of the Y chromosome: Relationship to race and length heteromorphism

J. V. Shah, R. Verma, H. Dosik, 1984, Heredity.

Size and pericentric inversion heteromorphisms of secondary constriction regions (h) of chromosomes 1, 9, and 16 as detected by CBG technique in Caucasians: classification, frequencies, and incidence.

H. Lubs, R. Verma, H. Dosik, 1978, American journal of medical genetics.

Inherited pericentric inversion of chromosome no. 2 with Robertsonian translocation (13q 14q) resulting in trisomy for chromosome 13q.

R. Verma, H. Dosik, I. Wexler, 1977, Journal de genetique humaine.

Human chromosomal heteromorphisms in American blacks. VI. Higher incidence of longer Y owing to non-fluorescent (nf) segment.

R. Verma, H. Dosik, M. Evans-McCalla, 1982, Journal of medical genetics.

Size variation polymorphisms of the short arm of human acrocentric chromosomes determined by R-banding by fluorescence using acridine orange (RFA)

H. Lubs, R. Verma, H. Dosik, 1977, Human Genetics.

Recent advances in detecting human chromosomal abnormalities by various banding techniques.

R. Verma, H. Dosik, 1982, Pathology annual.

Centromeric banding (C) of sequentially Q- and R-banded human chromosomes

R. Verma, H. Dosik, C. Rubenstein, 1978, Human Genetics.

The technical variables associated with the frequencies of QFQ, RFA and CBG heteromorphisms of human chromosomes

R. Verma, H. Dosik, 1979, Clinical genetics.

Primary amenorrhea in a black female with duplication and inversion of the secondary constriction regions of chromosome 9.

R. Verma, H. Dosik, J. Warman, 1978, The Journal of clinical endocrinology and metabolism.

Thiazide-induced immune hemolytic anemia.

H. Dosik, J. Vila, L. Blum, 1976, JAMA.

Haemolytic-uraemic syndrome following mumps vaccination.

H. Dosik, F. Tricárico, 1970, The Lancet.

Role of heterochromatin during preferential 9q;22q translocation in chronic myelogenous leukemia.

R. Silver, R. Verma, A. Babu, 1986, Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie.

Extramedullary presentation of blast crisis in chronic myelogenous leukemia.

R. Verma, H. Dosik, M. Krishnamurthy, 1985, Acta haematologica.

Acute pancreatitis in sickle cell crisis.

G. Posner, A. Kumar, H. Dosik, 1989, Journal of the National Medical Association.

Duplication 3q: severe manifestations in an infant with duplication of a short segment of 3q.

R. Verma, H. Evans, H. Dosik, 1981, American journal of medical genetics.

Partial Trisomy of Chromosome 3 (3q12 → qter) Owing to 3q/18p Translocation: A Trisomy 3q Syndrome

R. Verma, H. Dosik, R. Jhaveri, 1979 .

Frequencies of centromeric heteromorphisms of human chromosomes 3 and 4 as detected by QFQ technique: can they be identified by RFA technique?

R. Verma, H. Dosik, 1979, Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie.

A simplified technique for simultaneous staining of nucleolar organizer regions and kinetochores.

R. Verma, H. Dosik, S. Brat, 1979, Stain technology.

A possible cause of non-disjunction of additional chromosome 21 in Down syndrome

R. Verma, A. Babu, H. Dosik, 1986, Molecular and General Genetics MGG.

Expression of ribosomal cistrons of human chromosomes at high resolution.

J. V. Shah, R. Verma, H. Dosik, 1984, Stain technology.

Human chromosomal heteromorphisms in American blacks. IV. Intensity variation in centromeric regions of chromosomes 3 and 4.

R. Verma, H. Dosik, 1981, Canadian journal of genetics and cytology. Journal canadien de genetique et de cytologie.

48,XXX, plus 18 double trisomy.

H. Dosik, I. Wexler, D. P. Madahar, 1974, Journal of Medical Genetics.

A study of adult T‐cell leukemia/lymphoma incidence in central Brooklyn

E. Jaffe, P. Levine, A. Kahn, 1999, International journal of cancer.

17p+ in a patient with chronic myelogenous leukemia (CML): its differentiation from an isochromosome 17,[i(17q)].

R. Verma, H. Dosik, 1981, Cancer genetics and cytogenetics.

Effect of CO2 on short-term human lymphocyte culture in vitro

R. Verma, H. Dosik, C. Rubenstein, 1977, In Vitro.

Demonstration of color and size polymorphisms in human acrocentric chromosomes by acridine orange reverse banding.

H. Lubs, R. Verma, H. Dosik, 1977, The Journal of heredity.

Length polymorphisms of the human Y chromosome in patients with chronic myelogenous leukemia.

R. Silver, R. Verma, M. Coleman, 1987, Cancer genetics and cytogenetics.

Trisomy 21 in a child due to paternal nondisjunction as determined by RFA technique

R. Verma, H. Dosik, 1978, Japanese Journal of Human Genetics.

Chromatin ofh regions of human chromosomes at high resolution

R. Verma, H. Dosik, J. Rodriguez, 1984, Experientia.

Prevalence of HTLV‐I‐associated T‐cell lymphoma

A. Gottlieb, K. Rai, L. Ratner, 2001, American journal of hematology.

In vitro cultivation of human tumors: establishment of cell lines derived from a series of solid tumors.

S. Aaronson, D. Giard, G. Todaro, 1973, Journal of the National Cancer Institute.

Iron Deficiency Anemia in Adult Onset Still's Disease with a Serum Ferritin of 26,387 μg/L

A. Khalid, H. Dosik, Sheetal Patel, 2011, Anemia.

SV40 T-antigen expression in cultured fibroblasts from patients with Down syndrome and their parents.

W. Blattner, A. Lubiniecki, G. Martin, 1979, American journal of human genetics.

“Masked” Ph1-chromosome in chronic myelogenous leukaemia (CML)

R. Verma, H. Dosik, 1985, Blut.

Acute leukemia presenting as laryngeal obstruction

H. Dosik, M. Ti, Renato Villafuerte, 1974, Cancer.

Human chromosomal heteromorphisms in American Blacks VII. Correlation (r) between height and the size of the Y chromosome

R. Verma, H. Dosik, 1982, Japanese Journal of Human Genetics.

Variable X Chromosomal Abnormalities in Patients with Stigmata of Turner Syndrome

R. Verma, H. Dosik, Farida Khan, 1979, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.