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Primary shunt hyperbilirubinaemia in a large four-generation family confirming autosomal dominant genetic disorder
AIM: To describe the pattern of inheritance and confirm the diagnostic criteria of primary shunt hyperbilirubinaemia (PSH). METHODS: Forty members of a family pedigree across four generations were included in this study. All family members were interviewed and investigated by physical examination, h...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Baishideng Publishing Group Co., Limited
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4124395/ https://ncbi.nlm.nih.gov/pubmed/16718801 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3748/wjg.v12.i19.3123 |
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