Loading...
Charcot-Marie-Tooth disease type 1a (CMT1a): evidence for trisomy of the region p11.2 of chromosome 17 in south Wales families.
The gene for Charcot-Marie-Tooth disease type 1a (CMT1a) has been localised to chromosome 17p11.2. Locus D17S122 is recognised by the DNA probe pVAW409R3 which detects an MspI polymorphism with three alleles in the normal population. Subjects with CMT1a show evidence of trisomy for this region of ch...
Saved in:
| Published in: | J Med Genet |
|---|---|
| Main Authors: | , , |
| Format: | Artigo |
| Language: | Inglês |
| Published: |
BMJ Publishing Group
1992
|
| Subjects: | |
| Online Access: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC1015813/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1552536/ https://ncbi.nlm.nih.govhttps://doi.org/10.1136/jmg.29.1.12 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|