W. R. Breg

发表

Down syndrome: a review of recent progress in research.

W. R. Breg, 1977, Pathobiology annual.

Quinacrine fluorescence patterns and terminal DNA labelling of human C group chromosomes.

D. Miller, W. R. Breg, P. Alderdice, 1972, Nature: New biology.

Identification of translocation chromosomes by quinacrine fluorescence.

D. Miller, W. R. Breg, O. Miller, 1972, American journal of diseases of children.

Quinacrine Fluorescence Patterns of Human D Group Chromosomes

D. Miller, W. R. Breg, O. Miller, 1971, Nature.

Distinctive fluorescence of quinacrine-labelled human G group chromosomes.

D. Miller, W. R. Breg, O. Miller, 1971, Nature: New biology.

International Standing Committee on Human Cytogenetic Nomenclature

Y. Rumpler, Uta Francke, Elaine H. Zackai, 1976 .

Expression of H-Y antigen in human males with two Y chromosomes.

S. Wachtel, W. R. Breg, O. Miller, 1975, The New England journal of medicine.

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.

Xq–Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype

U. Surti, D. Page, B. Lahn, 1994, Nature Genetics.

Analysis of human Y-chromosome-specific reiterated DNA in chromosome variants.

L. Kunkel, S. Wachtel, W. R. Breg, 1977, Proceedings of the National Academy of Sciences of the United States of America.

Diagnosis of Angelman syndrome in infants.

W. R. Breg, J. S. Fryburg, V. Lindgren, 1991, American journal of medical genetics.

The cri du chat syndrome in adolescents and adults: clinical finding in 13 older patients with partial deletion of the short arm of chromosome No. 5(5p-).

W. R. Breg, O. Miller, P. Allderdice, 1970, The Journal of pediatrics.

Chromosome analysis of human amniotic-fluid cells.

W. R. Breg, M. Steele, 1966, Lancet.

Cytogenetic diagnosis using midtrimester fetal blood samples: application to suspected mosaicism and other diagnostic problems.

J. Hobbins, W. R. Breg, M. Watson, 1984, American journal of medical genetics.

Asynchronous DNA Replication and Discordant Length of Homologous Autosomes demonstrated by the Use of Markers

D. Miller, W. R. Breg, O. Miller, 1968, Nature.

Fragile X in a survey of 75 autistic males.

F. Volkmar, D. Cohen, J. Leckman, 1984, The New England journal of medicine.

Retinoblastoma and partial deletion of the long arm of chromosome 13.

W. R. Breg, O. Miller, D. Warburton, 1978, Transactions of the American Ophthalmological Society.

Mapping the locus of the H-Y gene on the human Y chromosome.

S. Wachtel, M. Genel, A. Miller, 1977, Science.

Human X chromosomes: Synchrony of DNA replication in diploid and triploid fibroblasts with multiple active or inactive X chromosomes

H. Willard, W. R. Breg, 1980, Somatic cell genetics.

NRAS transforming gene maps to region p11----p13 on chromosome 1 by in situ hybridization.

F. Ruddle, W. R. Breg, P. Barker, 1984, Cytogenetics and cell genetics.

CHROMOSOME DUPLICATION IN CULTURED LEUCOCYTES FROM PRESUMPTIVE XXX AND XXXXY HUMAN SUBJECTS.

W. R. Breg, O. Miller, B. B. Mukherjee, 1964, Experimental cell research.

Regional location of α1-antichymotrypsin and α1-antitrypsin genes on human chromosome 14

F. Ruddle, W. R. Breg, M. Watson, 1986 .

Angioimmunoblastic lymphadenopathy evolution to a Burkitt-like lymphoma.

W. R. Breg, D. Lovett, R. Enriquez, 1979, The American journal of medicine.

Loss of Rh antigen associated with acquired Rh antibodies and a chromosome translocation in a patient with myeloid metaplasia.

W. R. Breg, L. Atkins, P. Tishler, 1979, Blood.

Fragile X Syndrome

D. Cohen, R. Paul, W. R. Breg, 1984 .

Trisomy 8 mosaicism syndrome.

R. Ablow, W. R. Breg, R. Fineman, 1975, Pediatrics.

Retinoblastoma and chromosome abnormality. Partial deletion of the long arm of chromosome 13.

D. Albert, W. R. Breg, R. Lesser, 1974, Archives of ophthalmology.

Deletion (12)(q15q21.2).

W. R. Breg, M. Watson, M. Mahoney, 1989, Journal of medical genetics.

A family with an XXXXY male, a leukaemic male, and two 21-trisomic mongoloid females.

R. Schmickel, W. R. Breg, O. Miller, 1961, Lancet.

Fanconi's anemia: the preanemic phase.

A. Lubiniecki, W. R. Breg, S. Mcintosh, 1979, The American journal of pediatric hematology/oncology.

Complete trisomy 9 in two liveborn infants.

M. Seashore, W. R. Breg, J. Mcreynolds, 1981, Journal of medical genetics.

Ring chromosome 7 with variable phenotypic expression.

E. Zackai, W. R. Breg, 1973, Cytogenetics and cell genetics.

Fetal cystic hygroma. Cause and natural history.

R. Berkowitz, J. Hobbins, K. Blakemore, 1983, The New England journal of medicine.

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

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

Evidence for methylation of inactive human rRNA genes in amplified regions

W. R. Breg, O. Miller, B. Erlanger, 1981, Human Genetics.

Chromosomal translocations in patients with mongolism and in their normal relatives.

R. Schmickel, W. R. Breg, O. Miller, 1962, The New England journal of medicine.

Distribution of sex chromosome complements in 651 patients with turners syndrome

K. A. Clark, E. Hook, W. R. Breg, 1980 .

Human Thymidine Kinase Gene Locus: Assignment to Chromosome 17 in a Hybrid of Man and Mouse Cells

B. Migeon, D. Miller, W. R. Breg, 1971, Science.

Homogeneously staining region in a retinoblastoma cell line: relevance to tumor initiation and progression.

B. Gallie, W. R. Breg, F. Gilbert, 1981, Journal of the National Cancer Institute.

FAMILY COUNSELING IN DOWNS SYNDROME

W. R. Breg, 1970 .

Radioautographic identification of the D chromosomes involved in the centric fusion type of D/G translocation, t(DqGq)

W. R. Breg, O. Miller, A. Capoa, 1968, Annals of human genetics.

SECTION OF BIOLOGICAL AND MEDICAL SCIENCES: I. NORMAL VARIATIONS IN THE HUMAN KARYOTYPE*

W. R. Breg, O. Miller, B. B. Mukherjee, 1962 .

Summary of the 1993 ASHG ancillary meeting "recent research on chromosome 4p syndromes and genes".

D. Ledbetter, R. Myers, K. Hirschhorn, 1995, American journal of medical genetics.

Partial deletion of the short arm of chromosome no. 4(4p-): clinical studies in five unrelated patients.

D. Miller, H. Klinger, W. R. Breg, 1970, The Journal of pediatrics.

NON-RANDOM DISTRIBUTION OF CHROMOSOMES IN METAPHASE FIGURES FROM CULTURED HUMAN LEUCOCYTES. I. THE PERIPHERAL LOCATION OF THE Y CHROMOSOME.

W. R. Breg, O. Miller, B. B. Mukherjee, 1963, Cytogenetics.

NON-RANDOM DISTRIBUTION OF CHROMOSOMES IN METAPHASE FIGURES FROM CULTURED HUMAN LEUCOCYTES. II. THE PERIPHERAL LOCATION OF CHROMOSOMES 13, 17-18 AND 21.

W. R. Breg, O. Miller, B. B. Mukherjee, 1963, Cytogenetics.

Craniorachischisis in a partially trisomic 11 fetus in a family with reproductive failure and a reciprocal translocation, t(6p plus;11q minus).

W. R. Breg, W. E. Clark, Y. Wright, 1974, Journal of medical genetics.

A case of partial 14 trisomy 47,XY,(14q-)+ and translocation t(9p+;14q-) in mother and brother.

W. R. Breg, E. M. Short, G. Solitare, 1972, Journal of medical genetics.

Guidelines for the preparation and analysis of the fragile X chromosome in lymphocytes.

N. Spinner, J. Fryns, U. Froster-Iskenius, 1991, American journal of medical genetics.

Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15

W. R. Breg, O. Miller, B. Erlanger, 2004, Human Genetics.

Multilocus analysis of the fragile X syndrome

C. Schwartz, W. Brown, M. Krawczak, 1988, Human Genetics.

Familial occurrence of esophageal atresia with and without tracheoesophagel fistula: report of two unusual kindreds.

B. Pletcher, W. R. Breg, R. Touloukian, 1991, American journal of medical genetics.

21 Monosomy in a retarded female infant

W. R. Breg, Breg Wr, M. Mahoney, 1974, Journal of medical genetics.

Craniorachischisis in a Partially Trisomic 11 Fetus in a family with Reproductive Failure and a Reciprocal Translocation, t(6p+;11q−)

W. R. Breg, W. E. Clark, Y. Wright, 1974 .

A comparison of language characteristics of mentally retarded adults with fragile X syndrome and those with nonspecific mental retardation and autism

D. Cohen, R. Paul, J. Leckman, 1987, Journal of autism and developmental disorders.

Trisomy 22 mosaicism syndrome and Ullrich-Turner stigmata.

J. Graham, W. R. Breg, W. Wertelecki, 1986, American journal of medical genetics.

Standardization of procedures for chromosome studies in abortion.

A. Eidelman, W. R. Breg, R. Sparkes, 1966, Bulletin of the World Health Organization.

Fetal blood sampling and cytogenetic abnormalities

J. Hobbins, Chih-ping Chen, W. R. Breg, 1993, Prenatal diagnosis.

Unusual mosaicism of de novo structural abnormalities and ocular anomalies in a male with 13 trisomy syndrome.

W. R. Breg, R. Greenstein, R. O. Howard, 1981, American journal of medical genetics.

Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to partial 1q duplication and possible 18p deletion: a study of four individuals in two families.

L. Holmes, W. R. Breg, L. Atkins, 1979, American journal of medical genetics.

Chromosome deletion 1q42-43.

J. Gargus, K. Blakemore, W. R. Breg, 1986, American journal of medical genetics.

H-Y antigen expression in patients with X-autosomal translocations and gonadal dysgenesis.

U. Francke, W. R. Breg, F. Haseltine, 1982, American journal of medical genetics.

Quinacrine fluorescence for identifying metaphase chromosomes, with special reference to photomicrography.

W. R. Breg, 1972, Stain technology.

Report of two cases of distal deletion of the long arm of chromosome 6.

C. Stevens, W. R. Breg, R. Fineman, 1988, American journal of medical genetics.

DNA-based genetic testing in fifty fragile X families.

W. R. Breg, M. Watson, L. Shapiro, 1991, American journal of medical genetics.

Complete and partial trisomy of different segments of chromosome 8: case reports and review

R. Ablow, W. R. Breg, R. Fineman, 1979, Clinical genetics.

Partial deletion of short arm of chromosome no. 4.

W. R. Breg, J. Mace, M. Cunningham, 1971, The Journal of pediatrics.

Familial translocation involving chromosome 6, 14 and 20, identified by quinacrine fluorescence

D. Miller, W. R. Breg, P. Allderdice, 2004, Humangenetik.

A method of processing first-trimester chorionic villous biopsies for cytogenetic analysis.

K. Blakemore, W. R. Breg, M. Watson, 1984, American Journal of Human Genetics.

Chromosomal abnormality (46,XX,3p plus) in a case of the Meckel syndrome.

W. R. Breg, Y. Hsia, R. O. Howard, 1974, Birth defects original article series.

Maternal metaphases on direct chromosome preparation of first trimester decidua

K. Blakemore, W. R. Breg, M. Mahoney, 2004, Human Genetics.

Molecular and cytogenetic characterization of 9p- abnormalities.

M. Meyn, A. Teebi, W. R. Breg, 1993, American journal of medical genetics.

H-Y antigen in X,i(Xq) gonadal dysgenesis: Evidence of X-linked genes in testicular differentiation

S. Wachtel, M. Genel, W. R. Breg, 2004, Human Genetics.

Regional location of alpha 1-antichymotrypsin and alpha 1-antitrypsin genes on human chromosome 14.

F. Ruddle, W. R. Breg, M. Watson, 1986, Somatic cell and molecular genetics.

Translocation heterozygosis: a cause of five cases of the cri du chat syndrome and two cases with a duplication of chromosome number five in three families.

D. Miller, W. R. Breg, D. Warburton, 1967, American journal of human genetics.

Distinction between chromosome 4 and chromosome 5 by replication pattern and length of long and short arms.

D. Miller, M. Shaw, W. R. Breg, 1967, American journal of human genetics.

Alternative DNA replication patterns associated with long arm length of chromosomes 4 and 5 in the cri du chat syndrome.

K. Hirschhorn, D. Miller, W. R. Breg, 1966, Cytogenetics.

Duplication of euchromatin without phenotypic effects: a variant of chromosome 16.

W. R. Breg, T. Yang-Feng, C. Bryke, 1990, American journal of medical genetics.

A B-Group Ring Chromosome with Mosaicism in a Newborn with Cri du Chat Syndrome

A. Eidelman, W. R. Breg, M. Steele, 1966 .

Partial deletion o/the short arm of chromosome No 4(4t,-). Clinical ,t,di , i, unrelated patients

H. Klinger, W. R. Breg, D. Warburton, 1970 .

Deletion in the short arm of chromosome 9 from a subject with congenital cerebral maldevelopment. Repository identification No. GM-870.

W. R. Breg, A. Greene, L. Coriell, 1976, Cytogenetics and cell genetics.

Chromosome 3 duplication q/deletion p syndrome.

F. Hecht, R. Ablow, W. R. Breg, 1978, Pediatrics.

7q deletion syndrome (7q32 leads to 7qter).

M. Seashore, E. Harris, W. R. Breg, 1977, Clinical genetics.

H-Y antigen negative patients with testicular tissue and 46,XY karyotype

M. Genel, W. R. Breg, J. Crawford, 2004, Human Genetics.

Human c-fos oncogene mapped within chromosomal region 14q21----q31.

F. Ruddle, I. Verma, W. R. Breg, 1984, Proceedings of the National Academy of Sciences of the United States of America.

DELETED LATE-REPLICATING CHROMOSOME 4/5

W. R. Breg, A. Chutorian, Dorothy A. Miller, 1966 .

PRENATAL DETECTION OF TWO DIFFERENT MONOSOMIC CELL LINES BY CHORIONIC VILLUS SAMPLING

W. R. Breg, T. Yang-Feng, J. Copel, 1996, Prenatal diagnosis.

Aneuploidy and the fragile X syndrome.

W. Brown, D. Pauls, D. Meryash, 1988, American journal of medical genetics.

"Pseudomosaicism" for 4p- in amniotic fluid cell culture proven to be true mosaicism after birth.

J. Vockley, W. R. Breg, T. Yang-Feng, 1991, American journal of medical genetics.

Presence of H-Y antigen in patients with Ullrich-Turner syndrome and X-chromosome rearrangements.

M. Genel, W. R. Breg, K. Deponte, 1982, American journal of medical genetics.

Anthropometric comparison of mentally retarded males with and without the fragile X syndrome.

M. Butler, W. R. Breg, M. Watson, 1991, American journal of medical genetics.

Oocyte production in a Turner syndrome patient with serologically detectable male antigen.

M. Genel, W. R. Breg, F. Haseltine, 1984, Journal of reproductive immunology.

Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH).

E. Petty, W. R. Breg, T. Yang-Feng, 1993, American journal of medical genetics.

Experience with multiple approaches to the prenatal diagnosis of the fragile X syndrome: amniotic fluid, chorionic villi, fetal blood and molecular methods.

W. R. Breg, L. Shapiro, P. Murphy, 1988, American journal of medical genetics.

Anthropometric and craniofacial patterns in mentally retarded males with emphasis on the fragile X syndrome

M. Butler, W. R. Breg, M. Watson, 1993, Clinical genetics.

Evidence for the clonal origin of acquired hypomegakaryocytic thrombocytopenic purpura from a sex chromosome mosaic.

R. Hoffman, W. R. Breg, M. Cooper, 1984, Cancer genetics and cytogenetics.

Normal variations in the human karyotype.

W. R. Breg, B. B. Mukherjee, O. R. Miller, 1962, Transactions of the New York Academy of Sciences.

FISH diagnosis of partial trisomy 13 and tetrasomy 13 in a patient with severe trigonocephaly (C) phenotype.

A. Teebi, W. R. Breg, T. Yang-Feng, 1994, American journal of medical genetics.

Increased frequency of heterozygotes for α1 antitrypsin variants in individuals with either sex chromosome mosaicism or trisomy 21

K. Kidd, W. R. Breg, R. Fineman, 1976, Nature.

7q deletion syndrome (7q32→7qter)

W. R. Breg, M. Seashore, R. Wappner, 1977 .