Authors:
FREUND CL
WANG QL
CHEN SM
MUSKAT BL
WILES CD
SHEFFIELD VC
JACOBSON SG
MCINNES RR
ZACK DJ
STONE EM
Citation: Cl. Freund et al., DE-NOVO MUTATIONS IN THE CRX HOMEOBOX GENE ASSOCIATED WITH LEBER CONGENITAL AMAUROSIS, Nature genetics, 18(4), 1998, pp. 311-312
Authors:
JACOBSON SG
CIDECIYAN AV
HUANG YJ
HANNA DB
FREUND CL
AFFATIGATO LM
CARR RE
ZACK DJ
STONE EM
MCINNES RR
Citation: Sg. Jacobson et al., RETINAL DEGENERATIONS WITH TRUNCATION MUTATIONS IN THE CONE-ROD HOMEOBOX (CRX) GENE, Investigative ophthalmology & visual science, 39(12), 1998, pp. 2417-2426
Authors:
SOHOCKI MM
SULLIVAN LS
MINTZHITTNER HA
BIRCH D
HECKENLIVELY JR
FREUND CL
MCINNES RR
DAIGER SP
Citation: Mm. Sohocki et al., A RANGE OF CLINICAL PHENOTYPES ASSOCIATED WITH MUTATIONS IN CRX, A PHOTORECEPTOR TRANSCRIPTION-FACTOR GENE, American journal of human genetics, 63(5), 1998, pp. 1307-1315
Authors:
SWANSON DA
FREUND CL
STEEL JM
XU SB
PLODER L
MCINNES RR
VALLE D
Citation: Da. Swanson et al., A DIFFERENTIAL HYBRIDIZATION SCHEME TO IDENTIFY PHOTORECEPTOR-SPECIFIC GENES, PCR methods and applications, 7(5), 1997, pp. 513-521
Authors:
FREUND CL
GREGORYEVANS CY
FURUKAWA T
PAPAIOANNOU M
LOOSER J
PLODER L
BELLINGHAM J
NG D
HERBRICK JAS
DUNCAN A
SCHERER SW
TSUI LC
LOUTRADISANAGNOSTOU A
JACOBSON SG
CEPKO CL
BHATTACHARYA SS
MCINNES RR
Citation: Cl. Freund et al., CONE-ROD DYSTROPHY DUE TO MUTATIONS IN A NOVEL PHOTORECEPTOR-SPECIFICHOMEOBOX GENE (CRX) ESSENTIAL FOR MAINTENANCE OF THE PHOTORECEPTOR, Cell, 91(4), 1997, pp. 543-553
Authors:
FREUND CL
BELLINGHAM J
FURUKAWA T
LOOSER J
HERBRICK J
SCHERER S
TSUI LC
JACOBSON S
DUNCAN A
PAPAIOANNOU M
LOUTRADISANAGNOSTOU A
BHATTACHARYA S
CEPKO C
GREGORYEVANS CY
MCINNES RR
Citation: Cl. Freund et al., CONE-ROD DYSTROPHY DUE TO MUTATIONS IN A NOVEL PHOTORECEPTOR-SPECIFICHOMEOBOX GENE (CRX) REQUIRED FOR MAINTENANCE OF THE MAMMALIAN PHOTORECEPTOR, American journal of human genetics, 61(4), 1997, pp. 97-97
Authors:
SWANSON DA
FREUND CL
PLODER L
MCINNES RR
VALLE D
Citation: Da. Swanson et al., A UBIQUITIN C-TERMINAL HYDROLASE GENE ON THE PROXIMAL SHORT ARM OF THE X-CHROMOSOME - IMPLICATIONS FOR X-LINKED RETINAL DISORDERS, Human molecular genetics, 5(4), 1996, pp. 533-538