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Split hand/foot malformation genetics supports the chromosome 7 copy segregation mechanism for human limb development
Genetic aberrations of several unlinked loci cause human congenital split hand/foot malformation (SHFM) development. Mutations of the DLX5 (distal-less) transcription factor-encoding gene in chromosome 7 cause SHFM through haploinsufficiency, but the vast majority of cases result from heterozygous c...
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| Publicado no: | Philos Trans R Soc Lond B Biol Sci |
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| Autor principal: | |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Royal Society
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5104513/ https://ncbi.nlm.nih.gov/pubmed/27821526 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1098/rstb.2015.0415 |
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