Miller syndrome with novel dihydroorotate dehydrogenase gene mutations-Reference-Cited by-同舟云学术

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Miller syndrome with novel dihydroorotate dehydrogenase gene mutations

Published:2011-08 Issue:4 Volume:53 Page:587-591
ISSN:1328-8067
Container-title:Pediatrics International
language:en
Short-container-title:

Author:

Kinoshita Fumiko,Kondoh Tatsuro,Komori Kazuhiro,Matsui Takeshi,Harada Naoki,Yanai Akinori,Fukuda Masafumi,Morifuji Kanako,Matsumoto Tadashi

Publisher

Wiley

Subject

Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1442-200X.2010.03303.x/fullpdf

Reference10 articles.

1. Postaxial acrofacial dysostosis syndrome;Miller;J. Pediatr.,1979

2. Exome sequencing identifies the cause of a Mendelian disorder;Ng;Nat. Genet.,2010

3. Postaxial acrofacial dysostosis (Miller) syndrome;Donnai;J. Med. Genet.,1987

4. A family with dominant oculoauriculovertebral spectrum;Stoll;Am. J. Med. Genet.,1998

5. Treacher Collins syndrome;Dixon;Hum. Mol. Genet.,1996

Cited by 17 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Assessment of a novel variation in DHODH gene causing Miller syndrome: The first report in Chinese population;Molecular Genetics & Genomic Medicine;2023-04-30

2. Clinical and genomic features of non‐small cell lung cancer occurring in families;Thoracic Cancer;2023-03-03

3. Protein production, kinetic and biophysical characterization of three human dihydroorotate dehydrogenase mutants associated with Miller syndrome;Nucleosides, Nucleotides & Nucleic Acids;2022-01-30

4. DHODH and cancer: promising prospects to be explored;Cancer & Metabolism;2021-05-10

5. Broad‐spectrum next‐generation sequencing‐based diagnosis of a case of Nager syndrome;Journal of Clinical Laboratory Analysis;2020-06-14

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