Retinoic acid, cortisone, or thyroxine suppresses the mutant phenotype of the eyelid development mutation,lgMI, in mice
Author:
Publisher
Wiley
Subject
Animal Science and Zoology,General Medicine,Animal Science and Zoology,General Medicine
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1. Investigations of the genomic region that contains theclf1 mutation, a causal gene in multifactorial cleft lip and palate in mice;Birth Defects Research Part A: Clinical and Molecular Teratology;2005-02
2. Gaping lids, gp, a mutation on centromeric Chromosome 11 that causes defective eyelid development in mice;Mammalian Genome;2000-06
3. Mouse Mutants for Eye Development;Results and Problems in Cell Differentiation;2000
4. Retinal dysplasia and degeneration in RARbeta2/RARgamma2 compound mutant mice;Development;1996-07-01
5. The lidgap-Gates (lg Ga) mutation for open eyelids at birth maps to mouse Chromosome 13;Mammalian Genome;1996-06
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