FGF3-Related Phenotypes: A Study of LAMM Syndrome and Otodental Dysplasia Patients with Two Novel Mutations in FGF3 Gene
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Published:2020-08-05
Issue:04
Volume:20
Page:
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ISSN:0972-3757
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Container-title:INTERNATIONAL JOURNAL OF HUMAN GENETICS
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language:
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Short-container-title:IJHG
Author:
Turkyilmaz Ayberk
Publisher
Kamla Raj Enterprises
Subject
Genetics(clinical),Genetics