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Gleeson MJ (1984) Alport's syndrome: audiological manifestations and implica-
tions. J Laryngol Otol 98:449-465.
Goodenough DA, Goliger JA, Paul DL (1996) Connexins, connexons, and intercel-
lular communication. Annu Rev Biochem 65:475-502.
Goodman RM, Lewithal I, Solomon A, Klein D (1982) Upper limb involvement in
the Klein-Waardenburg syndrome. Am J Med Genet 11:425-433.
Gorlin RJ, Toriello HV, Cohen MM (1995) Hereditary hearing loss and its syn-
dromes. New York: Oxford University Press.
Goulding MD, Chalepakis G, Deutsch U, Erselius JR, Gruss P (1991) Pax-3, a novel
murine DNA binding protein expressed during early neurogenesis. Embo J
10:1135-1147.
Greenberg F, Elder FF, Haffner P, Northrup H, Ledbetter DH (1988) Cytogenetic
findings in a prospective series of patients with DiGeorge anomaly. Am J Hum
Genet 43:605-611.
Greinwald JH, Jr, Scott DA, Marietta JR, Carmi R, Manaligod J, Ramesh A, Zbar
RI, Kraft ML, Elbedour K, Yairi Y, Musy M, Skvorak AB, Van Camp G, Srisaila-
pathy CR, Lovett M, Morton CC, Sheffield VC, Smith RJ (1997) Construction of
P1-derived artificial chromosome and yeast artificial chromosome contigs encom-
passing the DFNB7 and DFNB11 region of chromosome 9q13-21. Genome Res
7:879-886.
Greinwald JH, Jr, Wayne S, Chen AH, Scott DA, Zbar RI, Kraft ML, Prasad S,
Ramesh A, Coucke P, Srisailapathy CR, Lovett M, Van Camp G, Smith RJ (1998)
Localization of a novel gene for nonsyndromic hearing loss (DFNB17) to
chromosome region 7q31. Am J Med Genet 78:107-113.
Grifa A, Wagner CA, D'Ambrosio L, Melchionda S, Bernardi F, Lopez-Bigas N,
Rabionet R, Arbones M, Monica MD, Estivill X, Zelante L, Lang F, Gasparini P
(1999) Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at
DFNA3 locus. Nat Genet 23:16-18.
Griffith AJ, Arts A, Downs C, Innis JW, Shepard NT, Sheldon S, Gebarski SS (1996)
Familial large vestibular aqueduct syndrome. Laryngoscope 106:960-965.
Griffith AJ, Chowdhry AA, Kurima K, Hood LJ, Keats BJ, Berlin CI, Morell RJ,
Friedman TB (2000a) Autosomal recessive nonsyndromic neuroscnsory deafness
at DFNB1 not associated with the compound-heterozygous GJB2 (Connexin 26)
genotype M34T/167delT. Am J Hum Genet 67:745-749.
Griffith AJ, Gebarski SS, Shepard NT, Kileny PR (2000b) Audiovestibular pheno-
type associated with a COL11A1 mutation in Marshall syndrome. Arch Oto-
laryngol Head Neck Surg 126:891-894.
Griffith AJ, Sprunger LK, Sirko-Osadsa DA, Tiller GE, Meisler MH, Warman ML
(1998) Marshall syndrome associated with a splicing defect at the COL11A1
locus. Am J Hum Genet 62:816-823.
Griffith AJ, Telian SA, Downs C, Gorski JL, Gebarski SS, Lalwani AK, Sheldon S
(1998) Familial Mondini dysplasia. Laryngoscope 108:1368-1373.
Guilford P, Ayadi H, Blanchard S, Chaib H, Le Paslier D, Weissenbach J, Drira M,
Petit C (1994b) A human gene responsible for neurosensory, non-syndromic
recessive deafness is a candidate homologue of the mouse sh-1 gene. Hum Mol
Genet 3:989-993.
Guilford P, Ben Arab S, Blanchard S, Levilliers J, Weissenbach J, Belkahia A, Petit
C (1994a) A non-syndrome form of neurosensory, recessive deafness maps to the
pericentromeric region of chromosome 13q. Nat Genet 6:24-28.
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