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A case of interstitial deletion of 10q25.2----q26.1.
A de novo interstitial deletion of chromosome 10, del(10)(pter----q25.2::q26.1----qter), was detected in a newborn female with facial anomalies, failure to thrive, and subsequent developmental delay. This case is compared with 10 previous reports of monosomy 10q within the q25----qter region. IMAGES...
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| Vydáno v: | J Med Genet |
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| Hlavní autoři: | , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
BMJ Publishing Group
1989
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1015539/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/2918528/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.26.1.58 |
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