Genomes and Genes
A J Griffith
Affiliation: Yale University
- Marshall syndrome associated with a splicing defect at the COL11A1 locusA J Griffith
Department of Human Genetics, University of Michigan, Ann Arbor, MI, USA
Am J Hum Genet 62:816-23. 1998..Our results also demonstrate allelism of Marshall syndrome with the subset of Stickler syndrome families associated with COL11A1 mutations...
- Optic, olfactory, and vestibular dysmorphogenesis in the homozygous mouse insertional mutant Tg9257A J Griffith
Department of Human Genetics, University of Michigan, Ann Arbor 48109 0618, USA
J Craniofac Genet Dev Biol 19:157-63. 1999..The 9257 mutation provides a model for analysis of the morphogenesis of these three neurosensory systems and their associated bony structures...
- Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPOA J Griffith
Department of Human Genetics, University of Michigan, Ann Arbor, Michigan, 48109, USA
Genomics 34:299-303. 1996..Obligatory recombinants were observed in 8 of the families, and negative lod scores from the other families indicated that these disorders are not linked to the chromosome 18 loci...