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Mburu P, Liu XZ, Walsh J, Saw D, Jr, Cope MJ, Gibson F, Kendrick-Jones J, Steel
KP, Brown SD (1997) Mutation analysis of the mouse myosin VIIA deafness gene.
Genes Funct 1:191-203.
McEvilly RJ, Erkman L, Luo L, Sawchenko PE, Ryan AF, Rosenfeld MG (1996)
Requirement for Brn-3.0 in differentiation and survival of sensory and motor
neurons. Nature 384:574-577.
McGuirt WT, Prasad SD, Griffith AJ, Kunst HP, Green GE, Shpargel KB, Runge C,
Huybrechts C, Mueller RF, Lynch E, King MC, Brunner HG, Cremers CW,
Takanosu M, Li SW, Arita M, Mayne R, Prockop DJ, Van Camp G, Smith RJ
(1999) Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13). Nat
Genet 23:413-419.
McKenna MJ, Kristiansen AG, Bartley ML, Rogus JJ, Haines JL (1998) Association
of COL1A1 and otosclerosis: Evidence for a shared genetic etiology with mild
osteogenesis imperfecta. Am J Otol 19:604-610.
McKenna MJ, Kristiansen AG, Haines J (1996) Polymerase chain reaction amplifi-
cation of a measles virus sequence from human temporal bone sections with
active otosclerosis. Am J Otol 17:827-830.
McKusick VA (1998) Mendelian Inheritance in Man, 10th edition. Baltimore: The
Johns Hopkins University Press.
Mermall V, Post PL, Mooseker MS (1998) Unconventional myosins in cell move-
ment, membrane traffic, and signal transduction. Science 279:527-533.
Miller GW, Joseph DJ, Cozad RL, McCabe BF (1970) Alport's syndrome. Arch
Otolaryngol 92:419-432.
Minowa O, Ikeda K, Sugitani Y, Oshima T, Nakai S, Katori Y, Suzuki M, Furukawa
M, Kawase T, Zheng Y, Ogura M, Asada Y, Watanabe K, Yamanaka H, Gotoh S,
Nishi-Takeshima M, Sugimoto T, Kikuchi T, Takasaka T, Noda T (1999) Altered
cochlear fibrocytes in a mouse model of DFN3 nonsyndromic deafness. Science
285:1408-1411.
Mochizuki T, Lemmink HH, Mariyama M, Antignac C, Gubler MC, Pirson Y,
Verellen-Dumoulin C, Chan B, Schroder CH, Smeets HJ, et al. (1994) Identifica-
tion of mutations in the alpha 3(IV) and alpha 4(IV) collagen genes in autoso-
mal recessive Alport syndrome. Nat Genet 8:77-81.
Mohr J, Mageroy K (1960) Sex-linked deafness of a possible new type. Acta Genet
Stat Med (Basel) 10:54-62.
Morell R, Friedman TB, Asher JH, Jr, Robbins LG (1997) The incidence of deaf-
ness is non-randomly distributed among families segregating for Waardenburg
syndrome type 1 (WS1). J Med Genet 34:447-452.
Morell R, Friedman TB, Moeljopawiro S, Hartono, Soewito, Asher JH, Jr (1992) A
frameshift mutation in the HuP2 paired domain of the probable human homolog
of murine Pax-3 is responsible for Waardenburg syndrome type 1 in an Indone-
sian family. Hum Mol Genet 1:243-247.
Morell R, Spritz RA, Ho L, Pierpont J, Guo W, Friedman TB, Asher JH, Jr (1997)
Apparent digenic inheritance of Waardenburg syndrome type 2 (WS2) and auto-
somal recessive ocular albinism (AROA). Hum Mol Genet 6:659-664.
Morell RJ, Friderici KH, Wei S, Elfenbein JL, Friedman TB, Fisher RA (2000) A
new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to
17q25. Genomics 63:1-6.
Morell RJ, Kim HJ, Hood LJ, Goforth L, Friderici K, Fisher R, Camp GV, Berlin
CI, Oddoux C, Ostrer H, Keats B, Friedman TB, Agustin TS, Dumon J (1998)
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