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Campomelic dysplasia associated with a de novo 2q;17q reciprocal translocation.
A phenotypically female fetus with campomelic dysplasia and a de novo reciprocal translocation, 46,XY,t(2;17) (q35;q23-24), is presented. This is the second case of campomelic dysplasia in which a rearrangement involving the long arm of chromosome 17 has been identified, indicating that this is like...
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| Publicado no: | J Med Genet |
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| Main Authors: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Publishing Group
1992
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1015925/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1583645/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.29.4.251 |
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