Pages that link to "Q40421008"
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The following pages link to A dinucleotide repeat polymorphism at the HOX2B locus (Q40421008):
Displaying 6 items.
- Assignment of the mulibrey nanism gene to 17q by linkage and linkage-disequilibrium analysis (Q24680481) (← links)
- The locus for Meckel syndrome with multiple congenital anomalies maps to chromosome 17q21-q24. (Q34294793) (← links)
- The G1021A substitution in the RYR1 gene does not cosegregate with malignant hyperthermia susceptibility in a British pedigree (Q35238558) (← links)
- A radiation hybrid map of the BRCA1 region (Q35889045) (← links)
- Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22. (Q35889804) (← links)
- Evolution of the HOXB6 intergenic region: motif conservation at the lateral plate mesoderm (LPM) enhancer element. (Q52914455) (← links)