(Q71985088)

English

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

scientific article published on 01 May 1995

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Europe PubMed Central

PubMed publication ID

7645589

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

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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)

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Europe PubMed Central

PubMed publication ID

7645589

reference URL

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

retrieved

22 October 2019

main subject

focal dermal hypoplasia

1 reference

Mücke J

1

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Europe PubMed Central

PubMed publication ID

7645589

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

retrieved

22 October 2019

Happle R

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2

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Europe PubMed Central

PubMed publication ID

7645589

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

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22 October 2019

Theile H

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3

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PubMed publication ID

7645589

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

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22 October 2019

publication date

1 May 1995

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7645589

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

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22 October 2019

published in

American Journal of Medical Genetics Part A

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PubMed publication ID

7645589

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

retrieved

22 October 2019

volume

57

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Europe PubMed Central

PubMed publication ID

7645589

reference URL

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

retrieved

22 October 2019

issue

1

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Europe PubMed Central

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7645589

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

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22 October 2019

page(s)

117-118

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7645589

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

retrieved

22 October 2019

Identifiers

DOI

10.1002/AJMG.1320570123

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Europe PubMed Central

PubMed publication ID

7645589

reference URL

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

retrieved

22 October 2019

PubMed publication ID

7645589

1 reference

stated in

Europe PubMed Central

PubMed publication ID

7645589

reference URL

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

(Q71985088)

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

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