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Del(3) (p25.3) without phenotypic effect.
A terminal deletion of chromosome 3 at p25.3 was observed during prenatal diagnosis. A similar deletion is also present in the phenotypically normal mother. The deletion was confirmed by FISH. The breakpoint is distal to the region responsible for the 3p- syndrome. A normal baby girl was born with n...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | English |
| Publicado: |
1995
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1051787/ https://ncbi.nlm.nih.gov/pubmed/8825934 |
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