A novel familial mutation associated with Treacher Collins syndrome: A case report-Reference-Cited by-同舟云学术

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A novel familial mutation associated with Treacher Collins syndrome: A case report

Published:2020-02-28 Issue: Volume: Page:
ISSN:2049-9434
Container-title:Biomedical Reports
language:
Short-container-title:biom rep

Author:

Papageorgiou Elena¹,Papoulidis Ioannis¹,Zavlanos Apostolos²,Papanikolaou Evaggelos³,Manolakos Emmanouil¹,Fidani Stiliani⁴

Affiliation:

1. Access to Genome, Clinical Laboratory Genetics, 55134 Thessaloniki, Greece

2. 1st Department of Obstetrics and Gynecology, Papageorgiou Hospital, 56403 Thessaloniki, Greece

3. 3rd Department of Obstetrics and Gynecology, Ippokratio Hospital, Aristotle University of Thessaloniki, 54642 Thessaloniki, Greece

4. Department for Special Needs, Aristotle University of Thessaloniki Achepa Hospital, 54636 Thessaloniki, Greece

Publisher

Spandidos Publications

Subject

General Pharmacology, Toxicology and Pharmaceutics,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Cited by 1 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. A systematic review on Treacher Collins syndrome: Correlation between molecular genetic findings and clinical severity;Clinical Genetics;2022-10-17

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