Hartsfield syndrome associated with a novel heterozygous missense mutation in FGFR1 and incorporating tumoral calcinosis.

2.50
Hdl Handle:
http://hdl.handle.net/11287/610463
Title:
Hartsfield syndrome associated with a novel heterozygous missense mutation in FGFR1 and incorporating tumoral calcinosis.
Authors:
Prasad, R.; Brewer, Carole; Burren, C. P.
Citation:
Hartsfield syndrome associated with a novel heterozygous missense mutation in FGFR1 and incorporating tumoral calcinosis. 2016 Aug;170(8):2222-5: Am. J. Med. Genet. A
Publisher:
Wiley
Journal:
American journal of medical genetics. Part A
Issue Date:
12-May-2016
URI:
http://hdl.handle.net/11287/610463
DOI:
10.1002/ajmg.a.37731
PubMed ID:
27170295
Additional Links:
http://dx.doi.org/10.1002/ajmg.a.37731
Type:
Letter
Language:
en
ISSN:
1552-4833
Appears in Collections:
Clinical Genetics (Peninsula Genetics); 2016 RD&E publications

Full metadata record

DC FieldValue Language
dc.contributor.authorPrasad, R.en
dc.contributor.authorBrewer, Caroleen
dc.contributor.authorBurren, C. P.en
dc.date.accessioned2016-05-20T15:25:15Zen
dc.date.available2016-05-20T15:25:15Zen
dc.date.issued2016-05-12en
dc.identifier.citationHartsfield syndrome associated with a novel heterozygous missense mutation in FGFR1 and incorporating tumoral calcinosis. 2016 Aug;170(8):2222-5: Am. J. Med. Genet. Aen
dc.identifier.issn1552-4833en
dc.identifier.pmid27170295en
dc.identifier.doi10.1002/ajmg.a.37731en
dc.identifier.urihttp://hdl.handle.net/11287/610463en
dc.languageENGen
dc.language.isoenen
dc.publisherWileyen
dc.relation.urlhttp://dx.doi.org/10.1002/ajmg.a.37731en
dc.rightsArchived with thanks to American journal of medical genetics. Part Aen
dc.subjectWessex Classification Subject Headings::Oncology. Pathology.::Geneticsen
dc.titleHartsfield syndrome associated with a novel heterozygous missense mutation in FGFR1 and incorporating tumoral calcinosis.en
dc.typeLetteren
dc.identifier.journalAmerican journal of medical genetics. Part Aen
dc.type.versionIn press (epub ahead of print)en
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