Authors:
JOOS KM
KIMURA AE
VANDENBURGH K
BARTLEY JA
STONE EM
Citation: Km. Joos et al., OCULAR FINDINGS ASSOCIATED WITH A CYS39ARG MUTATION IN THE NORRIE DISEASE GENE, Archives of ophthalmology, 112(12), 1994, pp. 1574-1579
Authors:
NICHOLS BE
DRACK AV
VANDENBURGH K
KIMURA AE
SHEFFIELD VC
STONE EM
Citation: Be. Nichols et al., A 2-BASE PAIR DELETION IN THE RDS GENE ASSOCIATED WITH BUTTERFLY-SHAPED PIGMENT DYSTROPHY OF THE FOVEA (VOL 2, PG 601, 1993), Human molecular genetics, 2(8), 1993, pp. 1347-1347
Authors:
NICHOLS BE
DRACK AV
VANDENBURGH K
KIMURA AE
SHEFFIELD VC
STONE EM
Citation: Be. Nichols et al., A 2 BASE-PAIR DELETION IN THE RDS GENE ASSOCIATED WITH BUTTERFLY-SHAPED PIGMENT DYSTROPHY OF THE FOVEA, Human molecular genetics, 2(5), 1993, pp. 601-603
Authors:
STONE EM
NICHOLS BE
KIMURA AE
WELEBER RG
GORIN MB
FISHMAN GA
JACOBSON SG
GASS JDM
DRACK AV
VANDENBURGH K
SHEFFIELD VC
Citation: Em. Stone et al., MUTATIONS IN THE RDS PERIPHERIN GENE CAUSE WIDELY DIFFERENT PHENOTYPES BETWEEN AND WITHIN AFFECTED FAMILIES, American journal of human genetics, 53(3), 1993, pp. 14-14
Authors:
BROWN DM
VANDENBURGH K
NICHOLS BE
ERHART AR
KIMURA AE
WEINGEIST TA
SHEFFIELD VC
STONE EM
Citation: Dm. Brown et al., GENETIC MUTATIONS AT THE C-TERMINAL END OF THE PROCOLLAGEN-II GENE INSTICKLER SYNDROME (HEREDITARY ARTHROOPHTHALMOPATHY) AND IDENTIFICATION AND PHENOTYPIC DESCRIPTION OF A NEW MUTATION, American journal of human genetics, 53(3), 1993, pp. 1133-1133