Whole-exome sequencing identified a homozygous FNBP4 mutation in a family with a condition similar to microphthalmia with limb anomalies (Q57147671)
Jump to navigation
Jump to search
No description defined
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Whole-exome sequencing identified a homozygous FNBP4 mutation in a family with a condition similar to microphthalmia with limb anomalies |
No description defined |
Statements
Whole-exome sequencing identified a homozygous FNBP4 mutation in a family with a condition similar to microphthalmia with limb anomalies (English)
0 references
July 2013
0 references
161A
0 references
7
0 references
1543-6
0 references
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference
1 reference