Wikidata

(Q77780271)

English

Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: possible localization of a neurofibromatosis type 2 modifier gene?

scientific article published on 01 June 1999

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Statements

title
Severe phenotype of neurofibromatosis type 2 in a patient with a 7.4-MB constitutional deletion on chromosome 22: possible localization of a neurofibromatosis type 2 modifier gene? (English)
1 reference
stated in
Europe PubMed Central
PubMed ID
10338003
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10338003%20AND%20SRC:MED&resulttype=core&format=json
retrieved
8 December 2019
author name string

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