(Q34633620)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5519605%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

title

Wolf-Hirschhorn syndrome associated with an unusual abnormality of chromosome no. 4 (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5519605%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

main subject

Wolf-Hirschhorn syndrome

1 reference

M G Wilson

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5519605%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

J W Towner

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5519605%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

L D Negus

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5519605%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

language of work or name

English

0 references

publication date

1 June 1970

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5519605%20AND%20SRC:MED&resulttype=core&format=json

Journal of Medical Genetics

20 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5519605%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

volume

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5519605%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

issue

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5519605%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

page(s)

164-170

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5519605%20AND%20SRC:MED&resulttype=core&format=json

PARTIAL DELETION OF SHORT ARMS OF CHROMOSOME NO. 5. REPORT OF A CASE IN A FRATERNAL TWIN.

20 October 2019

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468819

INTRAUTERINE GROWTH AS ESTIMATED FROM LIVEBORN BIRTH-WEIGHT DATA AT 24 TO 42 WEEKS OF GESTATION

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468819

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468819

Deletion of short arms of chromosome 4?5 in a child with defects of midline fusion

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468819

Deficiency on the short arms of a chromosome No. 4

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468819

Congenital malformations associated with a ring 4 chromosome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468819

Autosomal trisomy syndromes: a detailed study of 27 cases of Edwards' syndrome and 27 cases of Patau's syndrome

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1468819

[On a case of "crying cat" syndrome with peculiar phenotypic anomalies]

7 July 2018

1 reference

12 December 2020

Deleted late-replicating chromosomes

1 reference

12 December 2020

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

1 reference

12 December 2020

New syndrome associated with partial deletion of short arms of chromosome No. 4. Clinical manifestations of hypospadias, beaked nose, abnormal iris, hemangioma of forehead, seizures, and other anomalies

1 reference

12 December 2020

[New documents of delineation of a syndrome of the deletion of the short arm of one chromosome no 4]

1 reference

12 December 2020

IgA, IgM, and partial deletion of chromosome 18

1 reference

12 December 2020

[Francois's dyscephalic syndrome.]

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.7.2.164

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5519605%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:5519605%20AND%20SRC:MED&resulttype=core&format=json

20 October 2019

PubMed publication ID

5519605

1 reference