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Results: 1-6 |
Results: 6

Authors: STOCKTON DW LEWIS RA ABBOUD EB ALRAJHI A JABAK M ANDERSON KL LUPSKI JR
Citation: Dw. Stockton et al., A NOVEL LOCUS FOR LEBER CONGENITAL AMAUROSIS ON CHROMOSOME 14Q24, Human genetics, 103(3), 1998, pp. 328-333

Authors: DESILVA RN STOCKTON DW KEATS B JUSTICE CM RICHARDS CS ASHIZAWA T
Citation: Rn. Desilva et al., DELAYED DIAGNOSIS OF FRIEDREICHS ATAXIA DUE TO COEXISTING RECESSIVE DEAF BLIND SYNDROME/, Neurology, 50(6), 1998, pp. 1924-1925

Authors: ZHUCHENKO O BAILEY J BONNEN P ASHIZAWA T STOCKTON DW AMOS C DOBYNS WB SUBRAMONY SH ZOGHBI HY LEE CC
Citation: O. Zhuchenko et al., AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA (SCA6) ASSOCIATED WITH SMALL POLYGLUTAMINE EXPANSIONS IN THE ALPHA(1A)-VOLTAGE-DEPENDENT CALCIUM-CHANNEL, Nature genetics, 15(1), 1997, pp. 62-69

Authors: STOCKTON DW ROSS HL BACINO CA ALTMAN CA SHAFFER LG LUPSKI JR
Citation: Dw. Stockton et al., SEVERE CLINICAL PHENOTYPE DUE TO AN INTERSTITIAL DELETION OF THE SHORT ARM OF CHROMOSOME-1 - A BRIEF REVIEW, American journal of medical genetics, 71(2), 1997, pp. 189-193

Authors: LEE CC ZHUCHENKO O BAILEY J BONNEN P ASHIZAWA T STOCKTON DW AMOS C DOBYNS WB SUBRAMONY SH ZOGHBI HY
Citation: Cc. Lee et al., AUTOSOMAL-DOMINANT CEREBELLAR-ATAXIA (SCA6) ASSOCIATED WITH POLYGLUTAMINE EXPANSION IN THE ALPHA(1A)-VOLTAGE-DEPENDENT CALCIUM-CHANNEL, American journal of human genetics, 61(4), 1997, pp. 1829-1829

Authors: STOCKTON DW LEWIS RA ANDERSON KL ABBOUD EB ALRAJHI A LUPSKI JR
Citation: Dw. Stockton et al., MAPPING ADDITIONAL LOCI FOR LEBER CONGENITAL AMAUROSIS, American journal of human genetics, 61(4), 1997, pp. 2355-2355
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