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Results:
1-7
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Results: 7
Authors:
Auestad, N
Halter, R
Hall, RT
Blatter, M
Bogle, ML
Burks, W
Erickson, JR
Fitzgerald, KM
Dobson, V
Innis, SM
Singer, LT
Montalto, MB
Jacobs, JR
Qiu, WZ
Bornstein, MH
Citation: N. Auestad et al., Growth and development in term infants fed long-chain polyunsaturated fatty acids: A double-masked, randomized, parallel, prospective, multivariate study, PEDIATRICS, 108(2), 2001, pp. 372-381
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:
Baumgardner, RE
Isil, SS
Bowser, JJ
Fitzgerald, KM
Citation: Re. Baumgardner et al., Measurements of rural sulfur dioxide and particle sulfate: Analysis of CASTNet data, 1987 through 1996, J AIR WASTE, 49(11), 1999, pp. 1266-1279
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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