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Novel susceptibility locus at chromosome 6q16.3-22.31 in a family with GEFS+.
Genetic obesity syndromes.
Further delineation of interstitial chromosome 6 deletion syndrome and review of the literature.
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.
Interstitial deletion 6q16.2q22.2 in a child with ectrodactyly.