Phenotypic differences among patients with Bardet-Biedl syndrome linked to three different chromosome loci

Keyphrases

• Phenotypic Differences 100%
• Bardet-Biedl Syndrome 100%
• Chromosome Loci 100%
• Polydactyly 60%
• Chromosome 15 60%
• Obesity 40%
• Chromosome 3 40%
• Chromosome 16 40%
• Morbid Obesity 20%
• Bedouin Arabs 20%
• Intellectual Disability 20%
• Early Onset 20%
• Clinical Manifestations 20%
• Autosomal Recessive 20%
• Hypogenitalism 20%
• Linkage Mapping 20%
• Kindred 20%
• Human Obesity 20%
• Retinal Dystrophy 20%
• Cardiac Anomalies 20%
• Renal Abnormalities 20%
• Four Limbs 20%
• Postaxial Polydactyly 20%
• Limb Development 20%
• Obesity Genes 20%

Biochemistry, Genetics and Molecular Biology

• Chromosome 15 100%
• Chromosome 3 66%
• Chromosome 16 66%
• Limb Development 33%
• Gene Linkage 33%
• Autosomal Recessive Disorder 33%