(Q35231869)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240107%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

title

Short arm enlargement in acrocentric chromosomes (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240107%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

author name string

Sands VE

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240107%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

language of work or name

English

0 references

publication date

1 May 1969

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240107%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Human Genetics

24 September 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240107%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

volume

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240107%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240107%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

page(s)

293-304

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240107%20AND%20SRC:MED&resulttype=core&format=json

THE HUMAN CHROMOSOMAL SATELLITES IN NORMAL PERSONS AND IN TWO PATIENTS WITH MARFAN'S SYNDROME

24 September 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706413

A human skin culture technique used for cytological examinations

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706413

CYTOGENETICS OF DOWN'S SYNDROME (MONGOLISM). I. DATA ON A CONSECUTIVE SERIES OF PATIENTS REFERRED FOR GENETIC COUNSELLING AND DIAGNOSIS.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706413

ENLARGED CHROMOSOMAL SATELLITES ASSOCIATED WITH MENTAL RETARDATION AND DIGITAL ARCHES IN THREE GENERATIONS.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706413

Chromosomal abnormalities and their relation to disease.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706413

The demonstration of secondary constrictions in human chromosomes by means of a new technique

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706413

The satellited chromosomes of man with reference to the marfan syndrome.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706413

Enlarged satellites as a familial chromosome marker.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706413

Chromosome preparations of leukocytes cultured from human peripheral blood

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706413

A familial chromosome translocation associated with speech and mental retardation

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706413

Partial-trisomy syndromes. I. Sturge-Weber's disease.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706413

Familial occurrence of trisomy 22.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706413

Atypical acrocentric chromosomes in Negro and Caucasian Mongols

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706413

Chromosome studies on randomly chosen men and women.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706413

Pericentric inversion of chromosome 21. A possible further cytogenetic mechanism in mongolism

27 July 2018

1 reference

12 December 2020

The sites and relative frequencies of secondary constrictions in human somatic chromosomes

1 reference

12 December 2020

A child with an extra small metacentric chromosome

1 reference

12 December 2020

Enhancement of secondary constrictions and the heterochromatic X in human cells

1 reference

12 December 2020

ENLARGED SHORT ARM OR SATELLITE REGION-A HERITABLE TRAIT PROBABLY UNASSOCIATED WITH DEVELOPMENTAL DISORDER

1 reference

12 December 2020

THE ASSOCIATION OF SATELLITED CHROMOSOMES WITH SPECIFIC CHROMOSOMAL REGIONS IN CULTURED HUMAN SOMATIC CELLS

1 reference

12 December 2020

ENLARGED SHORT ARM OF A SMALL ACROCENTRIC CHROMOSOME IN GRANDFATHER, MOTHER AND CHILD, THE LATTER WITH DOWN'S SYNDROME

1 reference

12 December 2020

Normal variations in the human karyotype

1 reference

12 December 2020

Abnormal length of chromosomes 21 and 22 in four patients with Marfan's syndrome

1 reference

12 December 2020

A familial chromosome abnormality associated with repeated abortions

1 reference

12 December 2020

Enlarged satellites and multiple malformations in the same pedigree

1 reference

12 December 2020

FAMILIAL OCCURRENCE OF AN ABNORMAL D-CHROMOSOME

1 reference

12 December 2020

CHROMOSOME STUDIES IN MONGOLOIDS AND THEIR FAMILIES

1 reference

12 December 2020

Inheritance of marker chromosomes from a cytogenetic survey of congenital heart disease

1 reference

12 December 2020

Nucleolus-organisers in the causation of chromosomal anomalies in man

1 reference

12 December 2020

AN ABERRANT AUTOSOME (13-15) IN A HUMAN FEMALE AND HER FATHER, BOTH APPARENTLY NORMAL

1 reference

12 December 2020

CYTOGENETIC STUDIES IN LEUCOCYTES ON THE GENERAL POPULATION: SUBJECTS OF AGES 65 YEARS AND MORE

1 reference

12 December 2020

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:4240107%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

PubMed publication ID

4240107

1 reference