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Results:
1-15
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Results: 15
Authors:
Priston, M
Kozlowski, K
Gill, D
Letwin, K
Buys, Y
Levin, AV
Walter, MA
Heon, E
Citation: M. Priston et al., Functional analyses of two newly identified PITX2 mutants reveal a novel molecular mechanism for Axenfeld-Rieger syndrome, HUM MOL GEN, 10(16), 2001, pp. 1631-1638
Authors:
Friedmann, JS
Koop, BF
Raymond, V
Walter, MA
Citation: Js. Friedmann et al., Isolation of a ubiquitin-like (UBL5) gene from a screen identifying highlyexpressed and conserved iris genes, GENOMICS, 71(2), 2001, pp. 252-255
Authors:
Giordano, J
Prior, HM
Bamforth, JS
Walter, MA
Citation: J. Giordano et al., Genetic study of SOX9 in a case of campomelic dysplasia, AM J MED G, 98(2), 2001, pp. 176-181
Authors:
Vincent, A
Billingsley, G
Priston, M
Williams-Lyn, D
Sutherland, J
Glaser, T
Oliver, E
Walter, MA
Heathcote, G
Levin, A
Heon, E
Citation: A. Vincent et al., Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly, J MED GENET, 38(5), 2001, pp. 324-326
Authors:
Saleem, RA
Banerjee-Basu, S
Berry, FB
Baxevanis, AD
Walter, MA
Citation: Ra. Saleem et al., Analyses of the effects that disease-causing missense mutations have on the structure and function of the winged-helix protein FOXC1, AM J HU GEN, 68(3), 2001, pp. 627-641
Authors:
Mirzayans, F
Walter, MA
Citation: F. Mirzayans et Ma. Walter, Genomic mismatch scanning for the mapping of genetic traits, METH MOL B, 175, 2001, pp. 37-46
Authors:
Mirzayans, F
Gould, DB
Heon, E
Billingsley, GD
Cheung, JC
Mears, AJ
Walter, MA
Citation: F. Mirzayans et al., Axenfeld-Rieger syndrome resulting from mutation of the FKHL7 gene on chromosome 6p25, EUR J HUM G, 8(1), 2000, pp. 71-74
Authors:
Kozlowski, K
Walter, MA
Citation: K. Kozlowski et Ma. Walter, Variation in residual PITX2 activity underlies the phenotypic spectrum of anterior segment developmental disorders, HUM MOL GEN, 9(14), 2000, pp. 2131-2139
Authors:
Gould, DB
Walter, MA
Citation: Db. Gould et Ma. Walter, Cloning, characterization, localization, and mutational screening of the human BARX1 gene, GENOMICS, 68(3), 2000, pp. 336-342
Authors:
Friedman, JS
Ducharme, R
Raymond, V
Walter, MA
Citation: Js. Friedman et al., Isolation of a novel iris-specific and leucine-rich repeat protein (oculoglycan) using differential selection, INV OPHTH V, 41(8), 2000, pp. 2059-2066
Authors:
Walter, MA
Citation: Ma. Walter, A computer program for conducting incinerator risk assessments, DRUG CHEM T, 22(1), 1999, pp. 213-220
Authors:
Winnier, GE
Kume, T
Deng, KY
Rogers, R
Bundy, J
Raines, C
Walter, MA
Hogan, BLM
Conway, SJ
Citation: Ge. Winnier et al., Roles for the winged helix transcription factors MF1 and MFH1 in cardiovascular development revealed by nonallelic noncomplementation of null alleles, DEVELOP BIO, 213(2), 1999, pp. 418-431
Authors:
Friedman, JS
Walter, MA
Citation: Js. Friedman et Ma. Walter, Glaucoma genetics, present and future, CLIN GENET, 55(2), 1999, pp. 71-79
Authors:
Collison, ME
Stout, PJ
Glushko, TS
Pokela, KN
Mullins-Hirte, DJ
Racchini, JR
Walter, MA
Mecca, SP
Rundquist, J
Allen, JJ
Hilgers, ME
Hoegh, TB
Citation: Me. Collison et al., Analytical characterization of electrochemical biosensor test strips for measurement of glucose in low-volume interstitial fluid samples, CLIN CHEM, 45(9), 1999, pp. 1665-1673
Authors:
Tucker, JE
Winkfein, RJ
Murthy, SK
Friedman, JS
Walter, MA
Demetrick, DJ
Schnetkamp, PPM
Citation: Je. Tucker et al., Chromosomal localization and genomic organization of the human retinal rodNa-Ca+K exchanger, HUM GENET, 103(4), 1998, pp. 411-414
Risultati:
1-15
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