A J Griffith

Summary

Affiliation: Yale University
Country: USA

Publications

  1. pmc Marshall syndrome associated with a splicing defect at the COL11A1 locus
    A J Griffith
    Department of Human Genetics, University of Michigan, Ann Arbor, MI, USA
    Am J Hum Genet 62:816-23. 1998
  2. ncbi request reprint Optic, olfactory, and vestibular dysmorphogenesis in the homozygous mouse insertional mutant Tg9257
    A J Griffith
    Department of Human Genetics, University of Michigan, Ann Arbor 48109 0618, USA
    J Craniofac Genet Dev Biol 19:157-63. 1999
  3. ncbi request reprint Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPO
    A J Griffith
    Department of Human Genetics, University of Michigan, Ann Arbor, Michigan, 48109, USA
    Genomics 34:299-303. 1996

Collaborators

Detail Information

Publications3

  1. pmc Marshall syndrome associated with a splicing defect at the COL11A1 locus
    A 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...
  2. ncbi request reprint Optic, olfactory, and vestibular dysmorphogenesis in the homozygous mouse insertional mutant Tg9257
    A 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...
  3. ncbi request reprint Localization of the homolog of a mouse craniofacial mutant to human chromosome 18q11 and evaluation of linkage to human CLP and CPO
    A 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...