Source:http://linkedlifedata.com/resource/lhgdn/association:32400
| Predicate | Object |
|---|---|
| lhgdn:found_in | |
| lhgdn:geneRifSource |
This case report describes a novel polymorphism in the FMR1 gene that may cause difficulty in interpreting the Southern blot for diagnosis of fragile X syndrome.
|
| lhgdn:mesh_code |
D005600
|
| lhgdn:associationIdType | |
| lhgdn:umls_code |