Pages that link to "Q68206333"
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The following pages link to Physical mapping of two Xp markers DXS16 and DXS143 (Q68206333):
Displaying 2 items.
- Familial cases of a submicroscopic Xp22.2 deletion: genotype-phenotype correlation in microphthalmia with linear skin defects syndrome (Q36594323) (← links)
- Iridoschisis: high frequency ultrasound imaging. Evidence for a genetic defect? (Q37325189) (← links)