Expanding the spectrum of SMAD3 ‐related phenotypes to agnathia‐otocephaly-Reference-Cited by-同舟云学术

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Expanding the spectrum of SMAD3 ‐related phenotypes to agnathia‐otocephaly

Published:2020-02-26 Issue:4 Volume:8 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Meier Nicole¹²,Bruder Elisabeth³,Miny Peter¹,Tercanli Sevgi⁴,Filges Isabel¹²^ORCID

Affiliation:

1. Medical Genetics Institute of Medical Genetics and Pathology University Hospital Basel University of Basel Basel Switzerland

2. Department of Clinical Research University Hospital Basel Basel Switzerland

3. Pathology Institute of Medical Genetics and Pathology University Hospital Basel University of Basel Basel Switzerland

4. Centre for Prenatal Ultrasound Basel Switzerland

Funder

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1178

Reference26 articles.

1. Early-Onset Osteoarthritis, Charcot-Marie-Tooth Like Neuropathy, Autoimmune Features, Multiple Arterial Aneurysms and Dissections: An Unrecognized and Life Threatening Condition

2. Mutations in BMP4 Cause Eye, Brain, and Digit Developmental Anomalies: Overlap between the BMP4 and Hedgehog Signaling Pathways

3. A Smad3 transgenic reporter reveals TGF-beta control of zebrafish spinal cord development

4. PRRX1 is mutated in an otocephalic newborn infant conceived by consanguineous parents

5. Craniofacial defects in mice lacking BMP type I receptor Alk2 in neural crest cells

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