REPORT OF THE COMMITTEE ON CYTOGENETIC MARKERS

[1] AMAROSE AP, 1987, HUM GENET, V75, P4

[2] NONRANDOM DISTRIBUTION OF METHOTREXATE-INDUCED ABERRATIONS ON HUMAN-CHROMOSOMES - DETECTION OF FURTHER FOLIC-ACID SENSITIVE FRAGILE SITES [J]. HUMAN GENETICS, 1984, 68 (04) : 290 - 294

[3] REPORT OF THE COMMITTEE ON CHROMOSOME REARRANGEMENTS IN NEOPLASIA AND ON FRAGILE SITES [J]. CYTOGENETICS AND CELL GENETICS, 1985, 40 (1-4): : 490 - 535

[4] DEL(20P) WITH MANIFESTATIONS OF ARTERIOHEPATIC DYSPLASIA [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 24 (04): : 673 - 678

[5] CHODIRKER BN, 1987, CLIN GENET, V31, P1

[6] VARIATION IN THE EXPRESSION OF APHIDICOLIN-INDUCED FRAGILE SITES IN HUMAN-LYMPHOCYTE CULTURES [J]. HUMAN GENETICS, 1987, 76 (02) : 134 - 137

[7] CONSTITUTIVE FRAGILE SITES 1P31, 3P14, 6Q26, AND 16Q23 AND THEIR USE AS CONTROLS FOR FALSE-NEGATIVE RESULTS WITH THE FRAGILE(X) [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 18 (03): : 483 - 491

[8] A DELETION IN CHROMOSOME-22 CAN CAUSE DIGEORGE SYNDROME [J]. HUMAN GENETICS, 1981, 57 (03) : 253 - 256

[9] DUTRILLAUX B, 1985, ANN GENET-PARIS, V28, P161

[10] DEFICIENCY, TRANSPOSITION, AND DUPLICATION OF ONE 15Q REGION MAY BE ALTERNATIVELY ASSOCIATED WITH PRADER-WILLI (OR A SIMILAR) SYNDROME - ANALYSIS OF 7 CASES AFTER VARYING ASCERTAINMENT [J]. HUMAN GENETICS, 1983, 64 (04) : 388 - 394

[1] AMAROSE AP, 1987, HUM GENET, V75, P4

[2] NONRANDOM DISTRIBUTION OF METHOTREXATE-INDUCED ABERRATIONS ON HUMAN-CHROMOSOMES - DETECTION OF FURTHER FOLIC-ACID SENSITIVE FRAGILE SITES [J]. HUMAN GENETICS, 1984, 68 (04) : 290 - 294

[3] REPORT OF THE COMMITTEE ON CHROMOSOME REARRANGEMENTS IN NEOPLASIA AND ON FRAGILE SITES [J]. CYTOGENETICS AND CELL GENETICS, 1985, 40 (1-4): : 490 - 535

[4] DEL(20P) WITH MANIFESTATIONS OF ARTERIOHEPATIC DYSPLASIA [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1986, 24 (04): : 673 - 678

[5] CHODIRKER BN, 1987, CLIN GENET, V31, P1

[6] VARIATION IN THE EXPRESSION OF APHIDICOLIN-INDUCED FRAGILE SITES IN HUMAN-LYMPHOCYTE CULTURES [J]. HUMAN GENETICS, 1987, 76 (02) : 134 - 137

[7] CONSTITUTIVE FRAGILE SITES 1P31, 3P14, 6Q26, AND 16Q23 AND THEIR USE AS CONTROLS FOR FALSE-NEGATIVE RESULTS WITH THE FRAGILE(X) [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1984, 18 (03): : 483 - 491

[8] A DELETION IN CHROMOSOME-22 CAN CAUSE DIGEORGE SYNDROME [J]. HUMAN GENETICS, 1981, 57 (03) : 253 - 256

[9] DUTRILLAUX B, 1985, ANN GENET-PARIS, V28, P161

[10] DEFICIENCY, TRANSPOSITION, AND DUPLICATION OF ONE 15Q REGION MAY BE ALTERNATIVELY ASSOCIATED WITH PRADER-WILLI (OR A SIMILAR) SYNDROME - ANALYSIS OF 7 CASES AFTER VARYING ASCERTAINMENT [J]. HUMAN GENETICS, 1983, 64 (04) : 388 - 394