AAAAAA

   
Results: 1-8 |
Results: 8
CONCLUSIVE EVIDENCE FOR A DISTINCT CONGENITAL STATIONARY NIGHT BLINDNESS LOCUS IN XP21.1
Authors: BERGEN AAB TENBRINK JB RIEMSLAG F SCHUURMAN EJM MEIRE F TIJMES M DEJONG PTVM
Citation: Aab. Bergen et al., CONCLUSIVE EVIDENCE FOR A DISTINCT CONGENITAL STATIONARY NIGHT BLINDNESS LOCUS IN XP21.1, Journal of Medical Genetics, 33(10), 1996, pp. 869-872
MULTIPOINT LINKAGE ANALYSIS AND HOMOGENEITY TESTS IN 15 DUTCH X-LINKED RETINITIS-PIGMENTOSA FAMILIES
Authors: BERGEN AAB VANDENBORN LI SCHUURMAN EJM PINCKERS AJLG VANOMMEN GJB BLEEKERSWAGEMAKERS EM SANDKUIJL LA
Citation: Aab. Bergen et al., MULTIPOINT LINKAGE ANALYSIS AND HOMOGENEITY TESTS IN 15 DUTCH X-LINKED RETINITIS-PIGMENTOSA FAMILIES, Ophthalmic genetics, 16(2), 1995, pp. 63-70
LOCALIZATION OF A NOVEL X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS LOCUS - CLOSE LINKAGE TO THE RP3 TYPE RETINITIS-PIGMENTOSA GENE REGION
Authors: BERGEN AAB TENBRINK JB RIEMSLAG F SCHUURMAN EJM TIJMES N
Citation: Aab. Bergen et al., LOCALIZATION OF A NOVEL X-LINKED CONGENITAL STATIONARY NIGHT BLINDNESS LOCUS - CLOSE LINKAGE TO THE RP3 TYPE RETINITIS-PIGMENTOSA GENE REGION, Human molecular genetics, 4(5), 1995, pp. 931-935
CONSTRUCTION OF A TRANSCRIPTION MAP IN THE REGION OF THE RETINOSCHISIS DISEASE GENE
Authors: VANDEVOSSE E VANDERBENT P DATSON NA SCHUURMAN EJM BERGEN AAB VANOMMEN GJB DENDUNNEN JT
Citation: E. Vandevosse et al., CONSTRUCTION OF A TRANSCRIPTION MAP IN THE REGION OF THE RETINOSCHISIS DISEASE GENE, American journal of human genetics, 57(4), 1995, pp. 1988-1988
NANCE-HORAN SYNDROME - LINKAGE ANALYSIS IN A FAMILY FROM THE NETHERLANDS
Authors: BERGEN AAB TENBRINK J SCHUURMAN EJM BLEEKERWAGEMAKERS EM
Citation: Aab. Bergen et al., NANCE-HORAN SYNDROME - LINKAGE ANALYSIS IN A FAMILY FROM THE NETHERLANDS, Genomics, 21(1), 1994, pp. 238-240
DNA CARRIER DETECTION IN X-LINKED PROGRESSIVE CONE DYSTROPHY
Authors: BERGEN AAB MEIRE F SCHUURMAN EJM DELLEMAN JW
Citation: Aab. Bergen et al., DNA CARRIER DETECTION IN X-LINKED PROGRESSIVE CONE DYSTROPHY, Clinical genetics, 45(5), 1994, pp. 236-240
ADDITIONAL EVIDENCE FOR A GENE LOCUS FOR PROGRESSIVE CONE DYSTROPHY WITH LATE ROD INVOLVEMENT IN XP21.1-P11.3
Authors: BERGEN AAB MEIRE F TENBRINK J SCHUURMAN EJM VANOMMEN GJB DELLEMAN JW
Citation: Aab. Bergen et al., ADDITIONAL EVIDENCE FOR A GENE LOCUS FOR PROGRESSIVE CONE DYSTROPHY WITH LATE ROD INVOLVEMENT IN XP21.1-P11.3, Genomics, 18(2), 1993, pp. 463-464
CARRIER DETECTION IN X-LINKED OCULAR ALBINISM OF THE NETTLESHIP-FALLSTYPE BY DNA ANALYSIS
Authors: BERGEN AAB SCHUURMAN EJM VANDENBORN LI SAMANNS C VANDORP DB PINCKERS AJLG BAKKER E VANOMMEN GJB GAL A BLEEKERWAGEMAKERS EM
Citation: Aab. Bergen et al., CARRIER DETECTION IN X-LINKED OCULAR ALBINISM OF THE NETTLESHIP-FALLSTYPE BY DNA ANALYSIS, Clinical genetics, 41(3), 1992, pp. 135-138
Risultati: 1-8 |