Lataa...
The calcitonin-CGRP gene in the infantile hypercalcaemia/Williams-Beuren syndrome.
We have investigated 13 families, each of which have one member with infantile hypercalcaemia/Williams-Beuren syndrome (IHWBS), for either a germ cell mutation of, or an association with, the calcitonin-CGRP gene. Restriction fragment mapping studies of the calcitonin-CGRP gene using five restrictio...
Tallennettuna:
| Päätekijät: | , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
1989
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1015710/ https://ncbi.nlm.nih.gov/pubmed/2486208 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|