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Semilobar holoprosencephaly with 21q22 deletion: an autopsy report
Holoprosencephaly (HPE) is the most common forebrain developmental anomaly with a prevalence of 1:16 000 live-births. Possible aetiological agents include environmental factors and genetic defects such as trisomies (13, 18) and deletions (18p, 7q, 2p and 21q). This complex malformation is due to inc...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3962924/ https://ncbi.nlm.nih.gov/pubmed/24626384 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bcr-2014-203597 |
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