(Q68386059)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3377007%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

title

Variable expression of autosomal recessive polycystic kidney disease and congenital hepatic fibrosis within a family (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3377007%20AND%20SRC:MED&resulttype=core&format=json

autosomal recessive polycystic kidney

24 September 2019

main subject

1 reference

based on heuristic

inferred from title

Congenital hepatic fibrosis

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3377007

3 January 2023

author name string

Kaplan BS

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3377007%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

Kaplan P

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3377007%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

de Chadarevian JP

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3377007%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

Jequier S

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3377007%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

O'Regan S

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3377007%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

Russo P

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3377007%20AND%20SRC:MED&resulttype=core&format=json

24 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=3377007

3 January 2023

publication date

1 March 1988

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3377007%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

24 September 2019

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.1320290323

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320290323

https://onlinelibrary.wiley.com/doi/full/10.1002/ajmg.1320290323

3 January 2023

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320290323

American Journal of Medical Genetics Part A

3 January 2023

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3377007%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

volume

29

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3377007%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:3377007%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

page(s)

639-647

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3377007%20AND%20SRC:MED&resulttype=core&format=json

Polycystic disease of kidney and liver presenting in childhood

24 September 2019

cites work

7

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320290323

The spectrum of polycystic disease in children

3 January 2023

11

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320290323

Spectrum of anomalies in the Meckel syndrome, or: "Maybe there is a malformation syndrome with at least one constant anomaly"

3 January 2023

12

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320290323

Cystic disease of the kidneys. Autopsy report and family study

3 January 2023

14

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320290323

The renal lesion of congenital hepatic fibrosis: pathologic and morphometric analysis, with comparison to the renal lesion of infantile polycystic disease

3 January 2023

15

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320290323

Molecular analysis of the inheritance of phenylketonuria and mild hyperphenylalaninemia in families with both disorders

3 January 2023

19

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320290323

Infantile polycystic disease of the kidneys and liver: clinical, pathological and radiological correlations and comparison with congenital hepatic fibrosis

3 January 2023

20

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320290323

Polycystic kidneys in newborns, infants and children. A clinical and pathological study

3 January 2023

21

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320290323

Cystic disease of the kidney in the newborn infant

3 January 2023

25

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320290323

Cystic kidneys. Genetics, pathologic anatomy, clinical picture, and prenatal diagnosis

3 January 2023

27

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320290323

3 January 2023

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3377007%20AND%20SRC:MED&resulttype=core&format=json

24 September 2019

1 reference