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A new case of interstitial 6q16.2 deletion in a patient with Prader–Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity

New CaseGenetic DisorderGeneticsSim1 Gene DeletionPathologyComplex DiseaseMolecular GeneticsMedical GeneticsInterstitial 6Q16.2Disease Gene IdentificationGene ExpressionMedicineGene Deletion Data