Contiguous gene syndrome
(Q1128743)
Combined clinical phenotype caused by each missing gene in a chromosomal deletion
Combined clinical phenotype caused by each missing gene in a chromosomal deletion
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Current Data About
Contiguous gene syndrome
other details
| description | Combined clinical phenotype caused by each missing gene in a chromosomal deletion |
External Links
| (P646) |
/m/04gw41p
|
| (P2892) |
C1855496
|
| (P6366) |
2778329268
|