Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndrome-Reference-Cited by-同舟云学术

Primary lymphedema and other lymphatic anomalies are associated with 22q11.2 deletion syndrome

Published:2018-07 Issue:7 Volume:61 Page:411-415
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Unolt Marta^ORCID,Barry Jessica,Digilio Maria Cristina,Marino Bruno,Bassett Anne,Oechslin Erwin,Low David W.,Belasco Jean B.,Kallish Staci,Sullivan Kathleen,Zackai Elaine H.,McDonald–McGinn Donna M.

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

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5. Tbx1 regulates Vegfr3 and is required for lymphatic vessel development;Chen;J. Cell Biol.,2010

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3. A dual role for Tbx1 in cardiac lymphangiogenesis through genetic interaction with Vegfr3;The FASEB Journal;2020-09-20

4. Tbx1 interacts genetically with Vegfr3 to regulate cardiac lymphangiogenesis in mice;2019-02-18

5. A Novel Mutation of KIF11 in a Child with 22q11.2 Deletion Syndrome Associated with MCLMR;Molecular Syndromology;2018