(Q36599968)

15 August 2017

1 reference

title

Chromosome studies in man: past achievements and recent advances (English)

1 reference

15 August 2017

chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A789404

28 July 2022

author name string

S. D. Lawler

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A789404

28 July 2022

B. R. Reeves

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A789404

28 July 2022

language of work or name

English

0 references

publication date

1 July 1976

1 reference

PMC publication ID

476120

full work available at URL

15 August 2017

https://europepmc.org/articles/PMC476120

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A789404

https://europepmc.org/articles/PMC476120?pdf=render

28 July 2022

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A789404

Journal of Clinical Pathology

28 July 2022

published in

1 reference

15 August 2017

29

1 reference

15 August 2017

7

1 reference

15 August 2017

569-582

1 reference

THE SOMATIC CHROMOSOMAL CONSTITUTION OF SOME HUMAN SUBJECTS WITH GENETIC DEFECTS

15 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Multiple congenital anomaly caused by an extra autosome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

3 CASES OF PARTIAL DELETION OF THE SHORT ARM OF A 5 CHROMOSOME

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

An XYY man with progeny indicating familial tendency to non-disjunction

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

The chromosome constitution of a human phenotypic intersex.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

30 September 2017

A new trisomic syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Gene action in the X-chromosome of the mouse (Mus musculus L.)

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

A case of human intersexuality having a possible XXY sex-determining mechanism

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

30 September 2017

The Chromosomes of Man

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Aggressive behavior, mental sub-normality and the XYY male

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Possible differences between the karyotypes of preinvasive lesions and malignant tumours

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

A Special Role of the Group 17,18 Chromosomes in Reticuloendothelial Neoplasia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Assignment of the genes for malate oxidoreductase decarboxylating to chromosome 6 and peptidase B and lactate dehydrogenase B to chromosome 12 in man

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Distinct haematological disorder with deletion of long arm of no. 5 chromosome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Technique for identifying Y chromosomes in human interphase nuclei.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Sister chromatid exchanges, indices of human chromosome damage and repair: detection by fluorescence and induction by mitomycin C.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

An analysis of the break points of structural rearrangements in man

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Microfluorometric detection of deoxyribonucleic acid replication in human metaphase chromosomes

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Letter: A new consistent chromosomal abnormality in chronic myelogenous leukaemia identified by quinacrine fluorescence and Giemsa staining

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Polymorphism of human C-band heterochromatin. I. Frequency of variants

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Fluorescent staining of human chromosomes: identification of some common aberrations

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Identification of C trisomies in human abortuses

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Specific chromosome aberrations in ataxia telangiectasia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Human X-autosome translocations: differential inactivation of the X chromosome in a kindred with an X-9 translocation

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Nonrandom chromosomal abnormalities in hematologic disorders of man

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Transplacental passage of blood cells

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Previous reproductive history in mothers presenting with spontaneous abortions

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Cytological detection of mutagen-carcinogen exposure by sister chromatid exchange

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Sister chromatid exchange in human chromosomes from normal individuals and patients with ataxia telangiectasia

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

CHROMOSOMAL AUTORADIOGRAPHY IN THE CRI DU CHAT SYNDROME

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Racial differences in the length of the human Y chromosome

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Chromosome studies on workers exposed to atmospheric benzene. The possible influence of age.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Preferential location of x-ray induced chromosome breakage in the R-bands of human chromosomes

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Distribution of mitomycin C induced breaks on human chromosomes

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Identification of chromosome 9 in human male meiosis

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Cytogenetic studies in control men and women. I. Variations in aberration frequencies in 29,709 metaphases from 305 cultures obtained over a three-year period.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

High resolution studies on the pattern of induced exchanges in the human karyotype

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Origin of triploidy in human abortuses

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

On the specificity of the G abnormality in human meningomas studied by the fluorescence technique.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Radiation-induced non-random chromosome breakage

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Differentiation of X chromosomes by despiralization methods using 5-bromodeoxyuridine (BUDR) and controlled thermal denaturation

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Assignment of the major histocompatibility complex to chromosome No. 6 in a family with a pericentric inversion.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Localization of genes on human chromosomes by studies of human-Chinese hamster somatic cell hybrids. Assignment of PGM3 to chromosome C6 and regional mapping of the PGD, PGM1 and pep-C genes on chromosome A1.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

The Y chromosome in human spermatozoa.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Chromosome studies on 3500 newborn male infants.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

New Giemsa method for the differential staining of sister chromatids

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Preferential location of chlorambucil-induced breakage in the chromosomes of normal human lymphocytes.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Nonrandom distribution of chromosome breaks in Fanconi's anemia.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Letter: Marker-chromosome 14 in multiple myeloma and plasma-cell leukaemia

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

The effects of various banding procedures on human chromosomes, studied with acridine orange

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Retinoblastoma and D-chromosome deletions

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Staining of some specific regions of human chromosomes, particularly the secondary constriction of No. 9.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Alpha-fetoprotein in the antenatal diagnosis of anencephaly and spina bifida

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Marker band in one chromosome 14 from Burkitt lymphomas.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Cytological and cytogenetical studies on brain tumors. 4. Identification of the missing G chromosome in human meningiomas as no. 22 by fluorescence technique.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Detection of the X-chromatin body in human fibroblasts by quinacrine fluoromicroscopy.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Retinoblastoma and D-chromosome deletions.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Localization of heterochromatin in human chromosomes.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Sex-chromatin fluorescence in hair-root cells.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Quinacrine fluorescence of the human Y chromosome.

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Two pseudodiploid human breast carcinomas studied with G-band technique

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Chromosomes and causation of human cancer and leukemiaXII. Banding analysis of abnormal chromosomes in polycythemia vera

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Cytogenetics of Fetal Wastage

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Isochromosome 17 in Prostatic Cancer

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Cytological assessment of meiotic exchange in a human male with a pericentric inversion of chromosome No. 4

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Identification of the Philadelphia (Ph-1) chromosome

28 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Cytogenetics of malignant lymphomas. Studies utilising a Giemsa-banding technique.

20 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=476120

Sex-chromatin fluorescence in human amniotic-fluid cells

20 September 2018

1 reference

12 December 2020

A new technic of analysis of the human karyotype

1 reference

12 December 2020

A rapid banding technique for human chromosomes

1 reference

12 December 2020

New technique for distinguishing between human chromosomes

1 reference

12 December 2020

Cytological mapping of human chromosomes: results obtained with quinacrine fluorescence and the acetic-saline-Giemsa techniques

1 reference

12 December 2020

The 24 fluorescence patterns of the human metaphase chromosomes - distinguishing characters and variability

1 reference

12 December 2020

Identification of chromosome bivalents in human male meiosis by quinacrine mustard fluorescence analysis

1 reference

12 December 2020

DNA helical content during the C-banding procedure

1 reference

12 December 2020

Trisomy 8 in acute myeloid leukaemia

1 reference

12 December 2020

Chromosome banding studies in acute leukaemia at diagnosis

1 reference

12 December 2020

Identification of pachytene bivalents in human male meiosis using G-banding technique

1 reference

12 December 2020

Sister chromatid exchanges—A sensitive assay of agents damaging human chromosomes

1 reference

12 December 2020

Human Q and C chromosomal variations: distribution and incidence

1 reference

12 December 2020

A chromosome study of patients with uveitis treated with chlorambucil

1 reference

12 December 2020

Identification of the Philadelphia chromosome as a number 22 by quinacrine mustard fluorescence analysis

1 reference

12 December 2020

Chromosomes in the spinal fluid: evidence for metastatic origin of meningeal leukemia

1 reference

12 December 2020

Length variation in the quinacrine-binding segment of human Y chromosomes of different sizes

1 reference

12 December 2020

Polymorphism of Human Constitutive Heterochromatin

1 reference

12 December 2020

Chromosomal sex in the syndrome of testicular feminisation

1 reference

12 December 2020

A Mongol girl with 46 chromosomes

1 reference

12 December 2020

TIME CULTURE. AN IMPORTANT VARIABLE IN STUDYING IN VIVO RADIATION-INDUCED CHROMOSOME DAMAGE IN MAN

1 reference

12 December 2020

The No. 18 trisomy syndrome

1 reference

12 December 2020

Chromosomal abnormalities in father and Mongol child

1 reference

12 December 2020

A Presumptive Human XXY/XX Mosaic

1 reference

12 December 2020

Human Somatic Chromosomes

1 reference

12 December 2020

DNA banding patterns in carcinoma of the bladder

1 reference

12 December 2020

Molecular architecture of human chromosomes

1 reference

12 December 2020

Identification of isochromosome 17 in myeloid leukaemia

1 reference

12 December 2020

An analysis of the technical variables in the production of C bands

1 reference

12 December 2020

A simple technique for demonstrating centromeric heterochromatin

1 reference

12 December 2020

Differential Staining of Nucleolus Organisers in Mammalian Chromosomes

1 reference

12 December 2020

[New system of chromosome banding: the T bands (author's transl)]

1 reference

12 December 2020

Definitive Evidence for the Short Arm of the Y Chromosome associating with the X Chromosome during Meiosis in the Human Male

1 reference

12 December 2020

Multiple chromosome aberrations in a lymphosarcomatous tumor

1 reference

12 December 2020

Fluorescent staining of heteropycnotic chromosome regions in human interphase nuclei

1 reference

12 December 2020

Leukaemic transformation of engrafted human marrow cells in vivo

1 reference

12 December 2020

Chromosomal aberrations common to three types of monoclonal gammopathies

1 reference

12 December 2020

Chromosome analysis of human amniotic-fluid cells

1 reference

12 December 2020

Marrow grafting in patients with acute leukemia

1 reference

12 December 2020

Trisomy 21 in man due to maternal non-disjunction during the first meiotic division

1 reference

12 December 2020

Distinction between extra G-like chromosomes by quinacrine mustard fluorescence analysis

1 reference

12 December 2020

Quinacrine Fluorescence Patterns of Human D Group Chromosomes

1 reference

12 December 2020

Nonrandomness of translocations in man: preferential entry of chromosomes into 13-15-21 translocations

1 reference

12 December 2020

HL-A Antigens and Heteromorphic Fluorescence Characters of Chromosomes in Prenatal Paternity Investigation

1 reference

12 December 2020

Origin of the Philadelphia chromosome. Tracing of chromosome 22 to parents of patients with chronic myelocytic leukemia

1 reference

12 December 2020

Philadelphia-Chromosome Positive Bone-Marrow Cells Showing Loss of the Y in Males with Chronic Myeloid Leukaemia

1 reference

12 December 2020

Chromosome banding pattern in human colonic polyps

1 reference

12 December 2020

Linkage Analysis in Man by Somatic Cell Genetics

1 reference

12 December 2020

Identification of normal and abnormal chromosomes in tumor cells

1 reference

12 December 2020

Identity of the abnormal F-group chromosome associated with polycythaemia vera

1 reference

12 December 2020

Chromosome studies in acute leukemias developing in patients with multiple myeloma

1 reference

12 December 2020

Cytogenetic and cell-surface marker studies in two non-Hodgkin's lymphomata of T-cell origin

1 reference

12 December 2020

The Chromosomes of Bone‐Marrow Cells of Haematologically Normal Men and Women

1 reference

12 December 2020

The nature of structural X chromosome aberrations in Turner's syndrome as revealed by quinacrine mustard fluorescence analysis

1 reference

12 December 2020

Identification of the abnormal B group chromosome in the "cri du chat" syndrome by QM-fluorescence

1 reference

12 December 2020

Chromosome studies on bone marrow from a male control population

1 reference

12 December 2020

Chemical differentiation with fluorescent alkylating agents in Vicia faba metaphase chromosomes

1 reference

12 December 2020

Sex Chromosome Abnormalities in Two State Hospitals for Patients requiring Special Security

1 reference

12 December 2020

The Chromosomes in Polycythaemia Vera

1 reference

12 December 2020

Spontaneous chromosome aberrations in familial panmyelopathy

1 reference

12 December 2020

Identifiers

DOI

10.1136/JCP.29.7.569

1 reference

15 August 2017

1 reference

PMC publication ID

476120

15 August 2017

1 reference

PMC publication ID

476120