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146510
PHS
PALLISTER-HALL SYNDROME
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Chemical Phenomena
Biochemical Phenomena
Molecular Structure
Amino Acid Sequence
Base Sequence
Molecular Conformation
Protein Conformation
Protein Structure, Secondary
Amino Acid Motifs
Zinc Fingers
Genetic Phenomena
Genetic Processes
Gene Expression Regulation
Transcriptional Activation
Mutagenesis
Sequence Deletion
Translocation, Genetic
Recombination, Genetic
Transfection
Genetic Structures
Base Sequence
Chromosomes
Chromosomes, Mammalian
Chromosomes, Human
Chromosomes, Human, 6-12 and X
Chromosomes, Human, Pair 7
Genetic Code
Codon
Genome
Genome Components
DNA, Intergenic
Introns
Genes
Alleles
Gene Components
Codon
Exons
Introns
Genes, Dominant
Genes, Lethal
Genetic Variation
Mutation
Chromosome Aberrations
Mosaicism
Translocation, Genetic
Frameshift Mutation
Sequence Deletion
Polymorphism, Genetic
Polymorphism, Single-Stranded Conformational
Genotype
Inheritance Patterns
Genes, Dominant
Genetic Linkage
Phenotype
Genetic Markers
Reproductive and Urinary Physiological Phenomena
Reproductive Physiological Phenomena
Reproductive Physiological Processes
Reproduction
Pregnancy
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