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Duplication of the ZIC2 gene is not associated with holoprosencephaly
Cytogenetic testing using genomic microarrays presents a clinical challenge when data regarding the phenotypic consequences of the genomic alteration are not available. We describe a chromosome 13q32.3 duplication discovered by microarray testing in a fetus with a prenatally detected apparently bala...
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| Hlavní autoři: | , , , , , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2011
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3715301/ https://ncbi.nlm.nih.gov/pubmed/22105922 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.a.34375 |
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