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Meckel Gruber syndrome associated with anencephaly—an unusual reported case
Meckel–Gruber syndrome (MGS) is a rare and lethal ciliopathic disorder, with the incidence ranging between 1 in 13 000–400 000 live births. MGS is characterized by multisystem developmental malformations with the classical features of renal cystic dysplasia, occipital encephalocele and post-axial po...
Autores principales: | Yaqoubi, Houda Nasser Al, Fatema, Nishat |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5806412/ https://www.ncbi.nlm.nih.gov/pubmed/29479449 http://dx.doi.org/10.1093/omcr/omx092 |
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