FAMILIAL AORTOPATHIES
Testet das FBN1 gene encoding fibrillin 1 for Marfan syndrome, MASS (mitral valve, aorta, skeleton, and skin) syndrome, isolated ectopia lentis, Weill-Marchesani syndrome, and Shprintzen-Goldberg syndrome, TGFBR1 gene encoding transforming growth factor-beta recepto Gen
€ 1800
 | |
| Gen | FBN1 gene encoding fibrillin 1 for Marfan syndrome, MASS (mitral valve, aorta, skeleton, and skin) syndrome, isolated ectopia lentis, Weill-Marchesani syndrome, and Shprintzen-Goldberg syndrome, TGFBR1 gene encoding transforming growth factor-beta recepto |
| OMIM | |
| Tat | - |
| Methode | 6 genes |
| Prenatal | No |
| Order# | PGWD0821 |
