Lataa...
Mosaic partial trisomy 17q2.
Examination of an infant born after prenatal diagnosis of mosaic partial trisomy 17q2 showed the unique phenotypic features of this chromosomal abnormality, that is, frontal bossing, large mouth, brachyrhizomelia, and hexadactyly. Amniocentesis was performed because of polyhydramnios and ultrasound...
Tallennettuna:
| Julkaisussa: | J Med Genet |
|---|---|
| Päätekijät: | , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BMJ Publishing Group
1991
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1015800/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1956067/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.28.9.641 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|