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A New Spontaneous Mouse Mutation of Hoxd13 with a Polyalanine Expansion and Phenotype Similar to Human Synpolydactyly
by
Johnson, Kenneth R.
,
Sweet, Hope O.
,
Donahue, Leah Rae
,
Ward-Bailey, Pat
,
Bronson, Roderick T.
,
Davisson, Muriel T.
Published in
Human molecular genetics
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Human Molecular Genetics
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Abnormalities, Multiple - Genetics
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Amino Acid Sequence
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Animals
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Base Sequence
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Biochemistry & Molecular Biology
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Chromosome Mapping
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Diseases Of The Osteoarticular System
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Dna
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Dna Mutational Analysis
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Female
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Foot Deformities, Congenital - Embryology
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Foot Deformities, Congenital - Genetics
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Homeodomain Proteins - Genetics
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Humans
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Malformations And Congenital And Or Hereditary Diseases Involving Bones. Joint Deformations
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