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The genotype and phenotype of chromosome 18p deletion syndrome: Case series
RATIONALE: The chromosome 18p deletion syndrome is a syndrome with a deletion of all or a portion of the short arm of the chromosome 18. The phenotypes of the chromosome 18p deletion syndrome vary widely among individuals due to differences in size and breakpoints and the involved genes on the delet...
Gardado en:
| Publicado en: | Medicine (Baltimore) |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Lippincott Williams & Wilkins
2021
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8104293/ https://ncbi.nlm.nih.gov/pubmed/33950970 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000025777 |
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