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Partial and complete trisomy 14 mosaicism: clinical follow-up, cytogenetic and molecular analysis
BACKGROUND: Trisomy 14 mosaicism is a rare chromosomal abnormality. It is associated with multiple congenital anomalies. We report a 15 year-old female with an unusual karyotype with three cell lines: 47,XX,+mar/47,XX,+14/46,XX. At six months old she had short stature, cleft palate, hyperpigmented l...
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| Main Authors: | , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4180134/ https://ncbi.nlm.nih.gov/pubmed/25276227 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-014-0065-8 |
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