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- Identification of a Novel TAZ Gene Mutation in a Family with X-Linked
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- Genetics and Metabolics Abbreviations and Diagnosis
- Congenital Neutropenia and Primary Immunodeficiency Diseases
- Severe Course of Dilated Cardiomyopathy Associated with Duchenne Muscular Dystrophy (RCD Code: III‑1A.3A)
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- Neurological Diagnostic Criteria for Barth Syndrome
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- Barth Syndrome Clinic Factsheet
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- Review Article J Med Genet: First Published As 10.1136/Jmg.31.4.265 on 1 April 1994
- Genetics Fact Sheet the Barth Syndrome Foundation ( 5/28/2005~ Richard I
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- A Novel Alu-Mediated Xq28 Microdeletion Ablates TAZ and Partially Deletes DNL1L in a Patient with Barth Syndrome Harinder R
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- Neutropenia in Barth Syndrome: Characteristics, Risks, and Management
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- Do You Know About Barth Syndrome?
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