(Q71985088)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7645589%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

title

MIDAS syndrome respectively MLS syndrome: a separate entity rather than a particular lyonization pattern of the gene causing Goltz syndrome (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7645589%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

MIDAS syndrome respectively MLS syndrome: A separate entity rather than a particular lyonization pattern of the gene causing Goltz syndrome (English)

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320570123

11 July 2024

main subject

focal dermal hypoplasia

1 reference

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7645589

11 July 2024

author name string

J. Mücke

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7645589

11 July 2024

R. Happle

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7645589

11 July 2024

H. Theile

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7645589

11 July 2024

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=7645589

11 July 2024

publication date

1 May 1995

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7645589%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

22 May 1995

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7645589

full work available at URL

11 July 2024

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fajmg.1320570123

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320570123

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.1320570123

11 July 2024

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320570123

American Journal of Medical Genetics Part A

11 July 2024

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7645589%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

volume

57

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7645589%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7645589%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

page(s)

117-118

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7645589%20AND%20SRC:MED&resulttype=core&format=json

MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea): an X-linked phenotype distinct from Goltz syndrome

22 October 2019

cites work

1

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320570123

Microphthalmia with linear skin defects (MLS) syndrome: clinical, cytogenetic, and molecular characterization.

11 July 2024

2

1 reference

https://api.crossref.org/works/10.1002/AJMG.1320570123

11 July 2024

Identifiers

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7645589%20AND%20SRC:MED&resulttype=core&format=json

22 October 2019

1 reference