(Q68037812)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1519653%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

title

Xp22.3 microdeletion syndrome with microphthalmia, sclerocornea, linear skin defects, and congenital heart defects (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1519653%20AND%20SRC:MED&resulttype=core&format=json

Xp22.3 microdeletion syndrome

20 September 2019

main subject

microdeletion syndrome

1 reference

based on heuristic

inferred from title

1 reference

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1519653

chromosomal deletion syndrome

4 October 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1519653

4 October 2022

1

Lindor NM

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1519653%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

author name string

Michels VV

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1519653%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

Hoppe DA

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1519653%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

Driscoll DJ

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1519653%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

Leavitt JA

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1519653%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

Dewald GW

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1519653%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1519653

4 October 2022

publication date

1 September 1992

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1519653%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Medical Genetics Part A

20 September 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1519653%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

volume

44

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1519653%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1519653%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

page(s)

61-65

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1519653%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

Identifiers

DOI

10.1002/AJMG.1320440115

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1519653%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

1 reference