TRINUCLEOTIDE REPEAT INSTABILITY - WHEN AND WHERE

[1] MOLECULAR-BASIS OF MYOTONIC-DYSTROPHY - EXPANSION OF A TRINUCLEOTIDE (CTG) REPEAT AT THE 3' END OF A TRANSCRIPT ENCODING A PROTEIN-KINASE FAMILY MEMBER [J]. CELL, 1992, 68 (04) : 799 - 808

[2] BROOK JD, 1993, NAT GENET, V3, P279

[3] ANALYSIS OF FULL FRAGILE-X MUTATIONS IN FETAL TISSUES AND MONOZYGOTIC TWINS INDICATE THAT ABNORMAL METHYLATION AND SOMATIC HETEROGENEITY ARE ESTABLISHED EARLY IN DEVELOPMENT [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 43 (1-2): : 208 - 216

[4] VARIATION OF THE CGG REPEAT AT THE FRAGILE-X SITE RESULTS IN GENETIC INSTABILITY - RESOLUTION OF THE SHERMAN PARADOX [J]. CELL, 1991, 67 (06) : 1047 - 1058

[5] QUESTIONS OF EXPANSION [J]. NATURE GENETICS, 1993, 4 (01) : 8 - 9

[6] THE FULL MUTATION IN THE FMR-1 GENE OF MALE FRAGILE-X PATIENTS IS ABSENT IN THEIR SPERM [J]. NATURE GENETICS, 1993, 4 (02) : 143 - 146

[7] HERITABLE UNSTABLE DNA-SEQUENCES [J]. NATURE GENETICS, 1992, 1 (01) : 7 - 9

[8] DIRECT DIAGNOSIS BY DNA ANALYSIS OF THE FRAGILE X-SYNDROME OF MENTAL-RETARDATION [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (24) : 1673 - 1681

[9] SEGREGATION OF THE FRAGILE-X MUTATION FROM AN AFFECTED MALE TO HIS NORMAL DAUGHTER [J]. HUMAN MOLECULAR GENETICS, 1992, 1 (07) : 511 - 515

[10] MITOTIC STABILITY OF FRAGILE-X MUTATIONS IN DIFFERENTIATED CELLS INDICATES EARLY POSTCONCEPTIONAL TRINUCLEOTIDE REPEAT EXPANSION [J]. NATURE GENETICS, 1993, 4 (02) : 140 - 142

[1] MOLECULAR-BASIS OF MYOTONIC-DYSTROPHY - EXPANSION OF A TRINUCLEOTIDE (CTG) REPEAT AT THE 3' END OF A TRANSCRIPT ENCODING A PROTEIN-KINASE FAMILY MEMBER [J]. CELL, 1992, 68 (04) : 799 - 808

[2] BROOK JD, 1993, NAT GENET, V3, P279

[3] ANALYSIS OF FULL FRAGILE-X MUTATIONS IN FETAL TISSUES AND MONOZYGOTIC TWINS INDICATE THAT ABNORMAL METHYLATION AND SOMATIC HETEROGENEITY ARE ESTABLISHED EARLY IN DEVELOPMENT [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1992, 43 (1-2): : 208 - 216

[4] VARIATION OF THE CGG REPEAT AT THE FRAGILE-X SITE RESULTS IN GENETIC INSTABILITY - RESOLUTION OF THE SHERMAN PARADOX [J]. CELL, 1991, 67 (06) : 1047 - 1058

[5] QUESTIONS OF EXPANSION [J]. NATURE GENETICS, 1993, 4 (01) : 8 - 9

[6] THE FULL MUTATION IN THE FMR-1 GENE OF MALE FRAGILE-X PATIENTS IS ABSENT IN THEIR SPERM [J]. NATURE GENETICS, 1993, 4 (02) : 143 - 146

[7] HERITABLE UNSTABLE DNA-SEQUENCES [J]. NATURE GENETICS, 1992, 1 (01) : 7 - 9

[8] DIRECT DIAGNOSIS BY DNA ANALYSIS OF THE FRAGILE X-SYNDROME OF MENTAL-RETARDATION [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (24) : 1673 - 1681

[9] SEGREGATION OF THE FRAGILE-X MUTATION FROM AN AFFECTED MALE TO HIS NORMAL DAUGHTER [J]. HUMAN MOLECULAR GENETICS, 1992, 1 (07) : 511 - 515

[10] MITOTIC STABILITY OF FRAGILE-X MUTATIONS IN DIFFERENTIATED CELLS INDICATES EARLY POSTCONCEPTIONAL TRINUCLEOTIDE REPEAT EXPANSION [J]. NATURE GENETICS, 1993, 4 (02) : 140 - 142