Mutations of the P gene in oculocutaneous albinism, ocular albinism, and prader-willi syndrome plus albinism

Medicine and Dentistry

• Prader-Willi Syndrome 100%
• Oculocutaneous Albinism 80%
• Ocular Albinism 80%
• Albinism 60%
• Chromosome 40%
• Tyrosinase 40%
• Autosomal Recessive Inheritance 40%
• Polymerase Chain Reaction 20%
• DNA Sequencing 20%
• DNA 20%
• Polypeptide 20%
• Phenotype 20%
• Diseases 20%
• Melanin 20%
• Tyrosine 20%
• Precursor 20%
• Amino Acid Substitution 20%
• Exon 20%
• Glycine Dehydrogenase (Decarboxylating) 20%
• Missense Mutation 20%
• Autosomal Recessive Disorder 20%
• Heteroduplex 20%
• Angelman Syndrome 20%
• RNA Splicing 20%
• Chromosome 15q 20%
• Chromosome 15 20%

Agricultural and Biological Sciences

• Albinism 100%
• Mutation 71%
• Oculocutaneous Albinism 57%
• Chromosomes 28%
• Tyrosinase 28%
• Allele 20%
• DNA 14%
• Shotgun Sequencing 14%
• Polymorphism 14%
• Polypeptide 14%
• Phenotype 14%
• Rendering 14%
• Tyrosine 14%
• Polymerase Chain Reaction 14%
• Melanin 14%
• Amino Acid Substitution 14%
• RNA Splicing 14%
• Missense Mutation 14%

Neuroscience

• Prader Willi Syndrome 71%
• Chromosome 28%
• Phenotype 14%
• Melanin 14%
• Polymerase Chain Reaction 14%
• DNA 14%
• Tyrosine 14%
• Polymorphism 14%
• Autosomal Recessive Disorder 14%
• RNA Splicing 14%
• Angelman Syndrome 14%
• Missense Mutation 14%
• Chromosome 15q 14%
• DNA Sequencing 14%
• Chromosome 15 14%
• Exon 14%
• Heteroduplex 14%
• Glycine Dehydrogenase (Decarboxylating) 14%
• Amino Acid Substitution 14%