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MURCS association with situs inversus totalis: Expanding the spectrum or a novel disorder
We are reporting a female patient with a MURCS association (Müllerian duct aplasia, unilateral renal agenesis, cervico-thoracic somite fusion defects), situs inversus totalis, short stature with normal development and intelligence. We are presenting the comparison with two other patients published w...
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| Опубликовано в: : | J Pediatr Genet |
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| Главные авторы: | , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
Georg Thieme Verlag KG
2014
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| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5021002/ https://ncbi.nlm.nih.gov/pubmed/27625874 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3233/PGE-14096 |
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