Normal view MARC view ISBD view

Identity analysis of schwannomatosis kindreds with recurrent constitutional SMARCB1 (INI1) alterations.

Smith, M J

Identity analysis of schwannomatosis kindreds with recurrent constitutional SMARCB1 (INI1) alterations. [electronic resource] - Clinical genetics May 2009 - 501-2 p. digital

Publication Type: Letter

ISSN: 1399-0004

Standard No.: 10.1111/j.1399-0004.2009.01156.x doi

Subjects--Topical Terms:
Chromosomal Proteins, Non-Histone--genetics
DNA-Binding Proteins--genetics
Family
Haplotypes
Humans
Mutation, Missense
Neurilemmoma--genetics
SMARCB1 Protein
Transcription Factors--genetics

Print
Cite
Add to your cart (remove)
Save record
BIBTEX Dublin Core MARCXML MARC (non-Unicode/MARC-8) MARC (Unicode/UTF-8) MARC (Unicode/UTF-8, Standard) MODS (XML) RIS ISBD
More searches

Search for this title in:
Other Libraries (WorldCat) Other Databases (Google Scholar) Online Stores (Bookfinder.com) Open Library (openlibrary.org)