Found: 7
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Mutation of a Ubiquitously Expressed Mouse Transmembrane Protein (Tapt1) Causes Specific Skeletal Homeotic Transformations.
- Published in:
- Genetics, 2007, v. 175, n. 2, p. 699, doi. 10.1534/genetics.106.065177
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- Article
Phenotype-Based Identification of Mouse Chromosome Instability Mutants.
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- Genetics, 2003, v. 163, n. 3, p. 1031, doi. 10.1093/genetics/163.3.1031
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- Article
Inherited glaucoma in DBA/2J mice: Pertinent disease features for studying the neurodegeneration.
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- Visual Neuroscience, 2005, v. 22, n. 5, p. 637, doi. 10.1017/s0952523805225130
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- Article
Mouse models for the Wolf-Hirschhorn deletion syndrome.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 2, p. 91, doi. 10.1093/hmg/10.2.91
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- Article
Mouse models for the Wolf–Hirschhorn deletion syndrome.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 2, p. 91, doi. 10.1093/hmg/10.2.91
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- Article
Absence of glaucoma in DBA/2J mice homozygous for wild-type versions of Gpnmb and Tyrp1.
- Published in:
- BMC Genetics, 2007, v. 8, p. 1, doi. 10.1186/1471-2156-8-45
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- Article
An allele separating skeletal patterning and spermatogonial renewal functions of PLZF.
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- BMC Developmental Biology, 2010, v. 10, p. 33, doi. 10.1186/1471-213X-10-33
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- Article