FURTHER EVIDENCE FOR GENETIC-HETEROGENEITY IN THE FRAGILE-X SYNDROME

[21] JENKINS EC, 1981, LANCET, V2, P1292

[22] JENKINS EC, 1986, GENETIC DISORDERS FE, P185

[23] ANALYSIS OF THE FRAGILE-X CHROMOSOME - LOCALIZATION AND DETECTION OF THE FRAGILE SITE IN HIGH-RESOLUTION PREPARATIONS [J]. HUMAN GENETICS, 1985, 69 (03) : 209 - 211

[24] LANDOULSI A, 1985, Annales de Genetique, V28, P201

[25] LATHROP GM, 1984, AM J HUM GENET, V36, P460

[26] SOMATIC-CELL HYBRID STUDIES OF FRAGILE-(X) EXPRESSION IN A CARRIER FEMALE AND TRANSMITTING MALE [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (1-2): : 429 - 443

[27] MORTON NE, 1956, AM J HUM GENET, V8, P80

[28] 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

[29] THE TELOMERIC REGION OF THE HUMAN X-CHROMOSOME LONG ARM - PRESENCE OF A HIGHLY POLYMORPHIC DNA MARKER AND ANALYSIS OF RECOMBINATION FREQUENCY [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (09) : 2824 - 2828

[30] GENETIC-ANALYSIS OF THE FRAGILE-X MENTAL-RETARDATION SYNDROME WITH 2 FLANKING POLYMORPHIC DNA MARKERS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (04) : 1016 - 1020

[21] JENKINS EC, 1981, LANCET, V2, P1292

[22] JENKINS EC, 1986, GENETIC DISORDERS FE, P185

[23] ANALYSIS OF THE FRAGILE-X CHROMOSOME - LOCALIZATION AND DETECTION OF THE FRAGILE SITE IN HIGH-RESOLUTION PREPARATIONS [J]. HUMAN GENETICS, 1985, 69 (03) : 209 - 211

[24] LANDOULSI A, 1985, Annales de Genetique, V28, P201

[25] LATHROP GM, 1984, AM J HUM GENET, V36, P460

[26] SOMATIC-CELL HYBRID STUDIES OF FRAGILE-(X) EXPRESSION IN A CARRIER FEMALE AND TRANSMITTING MALE [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 23 (1-2): : 429 - 443

[27] MORTON NE, 1956, AM J HUM GENET, V8, P80

[28] 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

[29] THE TELOMERIC REGION OF THE HUMAN X-CHROMOSOME LONG ARM - PRESENCE OF A HIGHLY POLYMORPHIC DNA MARKER AND ANALYSIS OF RECOMBINATION FREQUENCY [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (09) : 2824 - 2828

[30] GENETIC-ANALYSIS OF THE FRAGILE-X MENTAL-RETARDATION SYNDROME WITH 2 FLANKING POLYMORPHIC DNA MARKERS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (04) : 1016 - 1020