THE CRITICAL REGION FOR ANGELMAN SYNDROME LIES BETWEEN D15S122 AND D15S113

[1] ANGELMAN H, 1965, DEV MED CHILD NEUROL, V7, P681

[2] BUITING K, 1993, HUM MOL GENET, V2, P1991

[3] ANGELMAN SYNDROME-ASSOCIATED WITH A MATERNAL 15Q11-13 DELETION OF LESS-THAN 200 KB [J]. HUMAN MOLECULAR GENETICS, 1994, 3 (08) : 1409 - 1413

[4] GREGER V, 1993, HUM MOL GENET, V7, P921

[5] Lalande Marc, 1993, V384, P225

[6] MALCOLM S, 1994, CYTOGENET CELL GENET, V67, P2

[7] LINKAGE ANALYSIS WITH CHROMOSOME-15Q11-13 MARKERS SHOWS GENOMIC IMPRINTING IN FAMILIAL ANGELMAN SYNDROME [J]. JOURNAL OF MEDICAL GENETICS, 1992, 29 (12) : 853 - 857

[8] A COMPLETE YAC CONTIG OF THE PRADER-WILLI/ANGELMAN CHROMOSOME REGION (15Q11-Q13) AND REFINED LOCALIZATION OF THE SNRPN GENE [J]. GENOMICS, 1993, 18 (03) : 546 - 552

[9] EXCLUSION OF THE GABA(A)-RECEPTOR-BETA-3 SUBUNIT GENE AS THE ANGELMANS SYNDROME GENE [J]. LANCET, 1993, 341 (8837) : 122 - 123

[10] WAGSTAFF J, 1993, AM J HUM GENET, V53, P105

[1] ANGELMAN H, 1965, DEV MED CHILD NEUROL, V7, P681

[2] BUITING K, 1993, HUM MOL GENET, V2, P1991

[3] ANGELMAN SYNDROME-ASSOCIATED WITH A MATERNAL 15Q11-13 DELETION OF LESS-THAN 200 KB [J]. HUMAN MOLECULAR GENETICS, 1994, 3 (08) : 1409 - 1413

[4] GREGER V, 1993, HUM MOL GENET, V7, P921

[5] Lalande Marc, 1993, V384, P225

[6] MALCOLM S, 1994, CYTOGENET CELL GENET, V67, P2

[7] LINKAGE ANALYSIS WITH CHROMOSOME-15Q11-13 MARKERS SHOWS GENOMIC IMPRINTING IN FAMILIAL ANGELMAN SYNDROME [J]. JOURNAL OF MEDICAL GENETICS, 1992, 29 (12) : 853 - 857

[8] A COMPLETE YAC CONTIG OF THE PRADER-WILLI/ANGELMAN CHROMOSOME REGION (15Q11-Q13) AND REFINED LOCALIZATION OF THE SNRPN GENE [J]. GENOMICS, 1993, 18 (03) : 546 - 552

[9] EXCLUSION OF THE GABA(A)-RECEPTOR-BETA-3 SUBUNIT GENE AS THE ANGELMANS SYNDROME GENE [J]. LANCET, 1993, 341 (8837) : 122 - 123

[10] WAGSTAFF J, 1993, AM J HUM GENET, V53, P105