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1. Towards a mutant map of the mouse – new models of neurological, behavioural, deafness, bone, renal and blood disorders

3. Novel phenotypes identified by plasma biochemical screening in the mouse

5. CCR2 and coronary artery disease: a woscops substudy

7. Finding genes in the web

8. Towards a mutant map of the mouse – new models of neurological, behavioural, deafness, bone, renal and blood disorders

12. Silicon Analogues of the Nonpeptidic GnRH Antagonist AG-045572: Syntheses, Crystal Structure Analyses, and Pharmacological Characterization

14. Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse

17. Towards a mutant map of the mouse ? new models of neurological, behavioural, deafness, bone, renal and blood disorders

18. Three Novel Pigmentation Mutants Generated by Genome-Wide Random ENU Mutagenesis in the Mouse

20. Mutation of Celsr1 Disrupts Planar Polarity of Inner Ear Hair Cells and Causes Severe Neural Tube Defects in the Mouse

21. A Mutation inAf4Is Predicted to Cause Cerebellar Ataxia and Cataracts in the Robotic Mouse

24. A systematic, genome-wide, phenotype-driven mutagenesis programme for gene function studies in the mouse

29. Bioinformatics for Geneticists

31. A Mutation in Af4 Is Predicted to Cause Cerebellar Ataxia and Cataracts in the Robotic Mouse.

32. Towards a mutant map of the mouse - new models of neurological, behavioural, deafness, bone, renal and blood disorders.

33. A 2.4-Megabase Physical Map Spanning the CYP2CGene Cluster on Chromosome 10q24

34. Single nucleotide polymorphisms as tools in human genetics.

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