(Q35231815)

7 August 2017

Localization of genes on chromosome 13: analysis of two kindreds (English)

1 reference

7 August 2017

human chromosomes 13-15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5703687

21 June 2023

chromosome abnormality

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5703687

21 June 2023

trisomy

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5703687

21 June 2023

author name string

G. E. Bloom

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5703687

21 June 2023

P. S. Gerald

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5703687

21 June 2023

language of work or name

English

0 references

publication date

1 November 1968

1 reference

full work available at URL

7 August 2017

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/5703687/?tool=EBI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5703687

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/5703687/pdf/?tool=EBI

21 June 2023

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5703687

https://europepmc.org/articles/PMC1706388

21 June 2023

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A5703687

https://europepmc.org/articles/PMC1706388?pdf=render

21 June 2023

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%3A5703687

American Journal of Human Genetics

21 June 2023

published in

1 reference

7 August 2017

20

1 reference

7 August 2017

495-511

1 reference

7 August 2017

6

1 reference

Multiple congenital anomaly caused by an extra autosome

7 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706388

THE PATTERN OF DNA SYNTHESIS IN THE CHROMOSOMES OF HUMAN BLOOD CELLS

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706388

DEVELOPMENTAL HEMOGLOBIN ANOMALIES IN A CHROMOSOMAL TRIPLICATION: D1 TRISOMY 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=1706388

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=1706388

Haptoglobin: a locus on the D1 chromosome?

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706388

A ring D chromosome and anomalous inheritance of haptoglobin type

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706388

Aneusomie de recombinaison: three further examples

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706388

A complex familial chromosome translocation

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706388

Studies on abnormal hemoglobins. I. Their demonstration in sickle cell anemia and other hematologic disorders by means of alkali denaturation.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1706388

On two familial cases of complex translocations

26 September 2018

1 reference

12 December 2020

Deoxyribonucleic acid replication and mapping of the D-1 chromosome. A study of two patients with partial trisomy D-1

1 reference

12 December 2020

Hematologic changes in the D1 trisomy syndrome

1 reference

12 December 2020

Ring D chromosome: a second case associated with anomalous haptoglobin inheritance

1 reference

12 December 2020

DNA REPLICATION PATTERNS OF HUMAN CHROMOSOMES

1 reference

12 December 2020

NUCLEAR ABNORMALITIES OF THE NEUTROPHILS IN D1 (13-15)-TRISOMY SYNDROME

1 reference

12 December 2020

FOETAL HAEMOGLOBIN AND NEUTROPHIL ANOMALY IN THE D1-TRISOMY SYNDROME

1 reference

12 December 2020

DEOXYRIBONUCLEIC-ACID REPLICATION PATTERN OF TRISOMY D1

1 reference

12 December 2020

CHARACTERIZATION OF GENETIC VARIANTS OF BLOOD PROTEINS

1 reference

12 December 2020

Identifiers

PMCID

1706388

1 reference

7 August 2017

1 reference