Publication | Open Access
Rubinstein-Taybi syndrome with deletions of FISH probe RT1 at 16p13.3: two UK patients.
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Citations
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References
1996
Year
Clinical DisordersRubinstein-taybi SyndromeMendelian DisorderCorticobasal DegenerationGenetic DisorderGeneticsInherited Metabolic DiseaseFish Probe Rt1PathologyMolecular MedicineCosmid Probe Rt1NeuropathologyMedicineTuberous SclerosisClinical Genetics
We report two patients with Rubinstein-Taybi syndrome out of a total of 16 tested who have a deletion of the region visualised by the cosmid probe RT1. These results further confirm this as a locus for Rubinstein-Taybi syndrome.
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