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Meckel Gruber Syndrome: Report of Two Cases with Review of Literature
Meckel Gruber syndrome (MKS) is a lethal, autosomal, recessive, multisystemic disorder, associated with mutations affecting ciliogenesis. Since the time it was first reported; only 200 cases have been reported. From January 2004 to December 2010, we evaluated 268 fetal autopsies in our institute, in...
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| Hlavní autoři: | , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Medknow Publications & Media Pvt Ltd
2013
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3894002/ https://ncbi.nlm.nih.gov/pubmed/24479060 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/2249-4863.109971 |
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