Filters: Department: "Human Genetics"
1 - 25 of 5
| Title | Date | Type | Setname | ||
|---|---|---|---|---|---|
| 1 |
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Role of hoxa1 in mammalian hindbrain, inner ear and neural crest development | 2010 | Text | ir_etd |
| 2 |
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Autosomal dominant cerebellar ataxia with retinal degeneration: clinical, neuropathologic, and genetic analysis of a large kindred. | 1994-08 | Text | ir_uspace |
| 3 |
 |
HOXB8 Microglia: origin, development and functions | 2018 | Text | ir_etd |
| 4 |
 |
Genetic and biochemical basis of familial advanced sleep phase syndrome in a Utah kindre | 2002-05 | Text | ir_etd |
| 5 |
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Spinocerebellar ataxia with retinal degeneration: from phenotype to gene to protein. | 2001-12 | Text | ir_etd |
1 - 25 of 5