FRAGILE-X SYNDROME

[1] BROWN WT, 1989, FRAGILE X SYNDROME

[2] LAIRD CD, 1989, AM J MED GENET, V30, P693

[3] ANTHROPOMETRY IN MARTIN-BELL SYNDROME [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1988, 30 (1-2): : 149 - 164

[4] CLINICAL-FEATURES AND REPRODUCTIVE PATTERNS IN FRAGILE-X FEMALE HETEROZYGOTES [J]. JOURNAL OF MEDICAL GENETICS, 1988, 25 (06) : 407 - 414

[5] RECOMBINATION AND AMPLIFICATION OF PYRIMIDINE-RICH SEQUENCES MAY BE RESPONSIBLE FOR INITIATION AND PROGRESSION OF THE XQ27 FRAGILE SITE - AN HYPOTHESIS [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (1-2): : 715 - 721

[6] A PRE-MUTATION THAT GENERATES A DEFECT AT CROSSING OVER EXPLAINS THE INHERITANCE OF FRAGILE X MENTAL RETARDATION [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 21 (04): : 709 - 717

[7] GENOMIC IMPRINTING AND GENETIC-DISORDERS IN MAN [J]. TRENDS IN GENETICS, 1989, 5 (10) : 331 - 336

[8] SHERMAN SL, 1988, AM J MED GENET, V30, P663

[9] Sutherland G, 1985, FRAGILE SITES HUMAN

[10] THAKE A, 1987, DEV MED CHILD NEUROL, V29, P711

[1] BROWN WT, 1989, FRAGILE X SYNDROME

[2] LAIRD CD, 1989, AM J MED GENET, V30, P693

[3] ANTHROPOMETRY IN MARTIN-BELL SYNDROME [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1988, 30 (1-2): : 149 - 164

[4] CLINICAL-FEATURES AND REPRODUCTIVE PATTERNS IN FRAGILE-X FEMALE HETEROZYGOTES [J]. JOURNAL OF MEDICAL GENETICS, 1988, 25 (06) : 407 - 414

[5] RECOMBINATION AND AMPLIFICATION OF PYRIMIDINE-RICH SEQUENCES MAY BE RESPONSIBLE FOR INITIATION AND PROGRESSION OF THE XQ27 FRAGILE SITE - AN HYPOTHESIS [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (1-2): : 715 - 721

[6] A PRE-MUTATION THAT GENERATES A DEFECT AT CROSSING OVER EXPLAINS THE INHERITANCE OF FRAGILE X MENTAL RETARDATION [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1985, 21 (04): : 709 - 717

[7] GENOMIC IMPRINTING AND GENETIC-DISORDERS IN MAN [J]. TRENDS IN GENETICS, 1989, 5 (10) : 331 - 336

[8] SHERMAN SL, 1988, AM J MED GENET, V30, P663

[9] Sutherland G, 1985, FRAGILE SITES HUMAN

[10] THAKE A, 1987, DEV MED CHILD NEUROL, V29, P711