Carregant...
Holoprosencephaly and sacral agenesis in a fetus with a terminal deletion 7q36-->7qter.
We describe here a fetus with holoprosencephaly and signs of caudal deficiency sequence. Chromosome examination showed a de novo balanced reciprocal translocation (7;22) (q36;q11) with loss of the derivative chromosome 22 in 50% of the cells examined. The present report and available published data...
Guardat en:
| Publicat a: | J Med Genet |
|---|---|
| Autors principals: | , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMJ Publishing Group
1993
|
| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1016431/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8326499/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.30.6.521 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|