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Phenotypic Variation between Monochorionic Diamniotic Twins with Coffin–Siris Syndrome
The first known documented case of monochorionic–diamniotic twins with Coffin–Siris syndrome is described in this study. This case is notable because of the phenotypic differences between infants despite having identical genomes and causative variants. Also unique to this case is the clinical influe...
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| Publicado no: | J Pediatr Genet |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Georg Thieme Verlag KG
2019
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6824890/ https://ncbi.nlm.nih.gov/pubmed/31687260 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-0039-1685500 |
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