Bardet–Biedl syndrome is linked to DNA markers on chromosome 11 q and is genetically heterogeneous

Medicine and Dentistry

• Syndrome 100%
• Chromosome 11 66%
• Family 66%
• Phenotype 33%
• Obesity 33%
• Genetic Heterogeneity 33%
• Autosomal Recessive Inheritance 33%
• Gene Linkage 33%
• Chromosome 11q 33%
• Retinopathy 33%
• Polydactyly 33%
• DNA Marker 33%
• Marker 33%
• Linkage Analysis 33%

Biochemistry, Genetics and Molecular Biology

• Chromosome 11 66%
• Mutation 33%
• Phenotype 33%
• Major Gene 33%
• Autosomal Recessive Inheritance 33%
• Mental Retardation 33%
• Chromosome 11q 33%
• Linkage Analysis 33%
• Genetic Heterogeneity 33%
• Genetic Marker 33%