HOMOZYGOSITY FOR FRAGILE SITE AT 17P12 IN A 28-YEAR-OLD HEALTHY MAN

[1] BERG JM, 1969, LANCET, V1, P531

[2] FRAGILE SITES IN CHROMOSOMES - POSSIBLE MODEL FOR THE STUDY OF SPONTANEOUS CHROMOSOME BREAKAGE [J]. SCIENCE, 1983, 220 (4592) : 69 - 70

[3] SCHERES JMJC, 1980, AM J HUM GENET, V32, P628

[4] DEMONSTRATION OF A HERITABLE FRAGILE SITE IN HUMAN CHROMOSOME-16 WITH DISTAMYCIN-A [J]. CYTOGENETICS AND CELL GENETICS, 1980, 28 (1-2): : 87 - 94

[5] A NEW FAMILIAL FRAGILE SITE ON CHROMOSOME 16 (Q23-24) - CYTOGENETIC AND CLINICAL CONSIDERATIONS [J]. HUMAN GENETICS, 1983, 64 (03) : 273 - 276

[6] SUTHERLAND GR, 1981, AM J HUM GENET, V33, P946

[7] SUTHERLAND GR, 1983, 15 INT C GEN NEW DEL, P68

[1] BERG JM, 1969, LANCET, V1, P531

[2] FRAGILE SITES IN CHROMOSOMES - POSSIBLE MODEL FOR THE STUDY OF SPONTANEOUS CHROMOSOME BREAKAGE [J]. SCIENCE, 1983, 220 (4592) : 69 - 70

[3] SCHERES JMJC, 1980, AM J HUM GENET, V32, P628

[4] DEMONSTRATION OF A HERITABLE FRAGILE SITE IN HUMAN CHROMOSOME-16 WITH DISTAMYCIN-A [J]. CYTOGENETICS AND CELL GENETICS, 1980, 28 (1-2): : 87 - 94

[5] A NEW FAMILIAL FRAGILE SITE ON CHROMOSOME 16 (Q23-24) - CYTOGENETIC AND CLINICAL CONSIDERATIONS [J]. HUMAN GENETICS, 1983, 64 (03) : 273 - 276

[6] SUTHERLAND GR, 1981, AM J HUM GENET, V33, P946

[7] SUTHERLAND GR, 1983, 15 INT C GEN NEW DEL, P68