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Ring chromosome 15 in a patient with features of Fryns' syndrome.
A stillborn male infant with a ring chromosome 15 and some features compatible with Fryns' syndrome is presented. Neither diagnosis is common and the overlap may be of significance.
Tallennettuna:
| Päätekijät: | , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
1989
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1015654/ https://ncbi.nlm.nih.gov/pubmed/2746621 |
| Tagit: |
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