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Genetic analysis of chromosome 22q11.2 markers in congenital heart disease
Congenital heart disease (CHD) is a common cardiac defect found in infants and children. Despite advances in diagnosis and treatment, our understanding of the causative mechanism and etiology of CHD is limited. To determine the genetic etiology of CHD, we selected 11 consecutive short tandem‐repeat...
Gardado en:
| Publicado en: | J Clin Lab Anal |
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| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Wiley Subscription Services, Inc., A Wiley Company
2003
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6807742/ https://ncbi.nlm.nih.gov/pubmed/12526020 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.10062 |
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