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Results:
1-7
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Results: 7
Authors:
Donoso, LA
Frost, AT
Stone, EM
Weleber, RG
MacDonald, IM
Hageman, GS
Cibis, GW
Ritter, R
Edwards, AO
Citation: La. Donoso et al., Autosomal dominant Stargardt-like macular dystrophy - Founder effect and reassessment of genetic heterogeneity, ARCH OPHTH, 119(4), 2001, pp. 564-570
Authors:
Fitzgerald, KM
Hashimoto, T
Hug, TE
Cibis, GW
Harris, DJ
Citation: Km. Fitzgerald et al., Autosomal dominant inheritance of a negative electroretinogram phenotype in three generations, AM J OPHTH, 131(4), 2001, pp. 495-502
Authors:
Hug, TE
Fitzgerald, KM
Cibis, GW
Citation: Te. Hug et al., Clinical and electroretinographic findings in fetal alcohol syndrome, J AAPOS, 4(4), 2000, pp. 200-204
Authors:
Smith, DE
Fitzgerald, K
Stass-Isern, M
Cibis, GW
Citation: De. Smith et al., Electroretinography is necessary for spasmus nutans diagnosis, PED NEUROL, 23(1), 2000, pp. 33-36
Authors:
Pillers, DAH
Fitzgerald, KM
Duncan, NM
Rash, SM
White, RA
Dwinnell, SJ
Powell, BR
Schnur, RE
Ray, PN
Cibis, GW
Weleber, RG
Citation: Dah. Pillers et al., Duchenne/Becker muscular dystrophy: correlation of phenotype by electroretinography with sites of dystrophin mutations, HUM GENET, 105(1-2), 1999, pp. 2-9
Authors:
Fitzgerald, KM
Cibis, GW
Gettel, AH
Rinaldi, R
Harris, DJ
White, RA
Citation: Km. Fitzgerald et al., ERG phenotype of a dystrophin mutation in heterozygous female carriers of Duchenne muscular dystrophy, J MED GENET, 36(4), 1999, pp. 316-322
Authors:
Fitzgerald, KM
Cibis, GW
White, RA
Citation: Km. Fitzgerald et al., ERG in Duchenne/Becker muscular dystrophy, PED NEUROL, 19(5), 1998, pp. 400-400
Risultati:
1-7
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