Found: 5
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Early-progressive dilated cardiomyopathy in a family with Becker muscular dystrophy related to a novel frameshift mutation in the dystrophin gene exon 27.
- Published in:
- Journal of Human Genetics, 2015, v. 60, n. 3, p. 151, doi. 10.1038/jhg.2014.112
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- Publication type:
- Article
Genetic counseling for congenital heart disease – Practice resource of the National Society of Genetic Counselors.
- Published in:
- Journal of Genetic Counseling, 2022, v. 31, n. 1, p. 9, doi. 10.1002/jgc4.1498
- By:
- Publication type:
- Article
Novel SMAD3 Mutation in a Patient with Hypoplastic Left Heart Syndrome with Significant Aortic Aneurysm.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
Sudden cardiac death in children and young adults without structural heart disease: a comprehensive review.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Inherited intragenic PBX1 deletion: Expanding the phenotype.
- Published in:
- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 1, p. 234, doi. 10.1002/ajmg.a.61932
- By:
- Publication type:
- Article