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Sprouty loss of function mutations in the mouse results in defects characteristic of 22q11 deletion syndrome, which are exacerbated by Tbx1 haploinsufficiency

Title: Sprouty loss of function mutations in the mouse results in defects characteristic of 22q11 deletion syndrome, which are exacerbated by Tbx1 haploinsufficiency
Authors: Simrick, Subreena; Szumska, Dorota; Gardiner, Jennifer; Karun, Sagar; Morrow, Bernice; Bhattacharya, Shoumo; Basson, Michiel A.
Source: Developmental Biology ; volume 356, issue 1, page 223-224 ; ISSN 0012-1606
Publisher Information: Elsevier BV
Publication Year: 2011
Collection: ScienceDirect (Elsevier - Open Access Articles via Crossref)
Document Type: article in journal/newspaper
Language: English
DOI: 10.1016/j.ydbio.2011.05.366
Availability: http://dx.doi.org/10.1016/j.ydbio.2011.05.366; https://api.elsevier.com/content/article/PII:S0012160611006634?httpAccept=text/xml; https://api.elsevier.com/content/article/PII:S0012160611006634?httpAccept=text/plain
Rights: https://www.elsevier.com/tdm/userlicense/1.0/ ; http://www.elsevier.com/open-access/userlicense/1.0/
Accession Number: edsbas.2E53F245
Database: BASE