HIGH-RESOLUTION CHROMOSOME ANALYSIS .1. APPLICATIONS AND LIMITATIONS

[1] HIGH-RESOLUTION IN SITU HYBRIDIZATION TECHNIQUE FOR THE DIRECT VISUALIZATION OF LABELED G-BANDED EARLY METAPHASE AND PROPHASE CHROMOSOMES [J]. CYTOGENETICS AND CELL GENETICS, 1978, 22 (1-6): : 352 - 356

[2] ANIRIDIA-WILMS TUMOR ASSOCIATION - EVIDENCE FOR SPECIFIC DELETION OF 11P13 [J]. CYTOGENETICS AND CELL GENETICS, 1979, 24 (03): : 185 - 192

[3] FRANCKE U, 1977, CYTOGENET CELL GENET, V19, P107

[4] FACTORS INVOLVED IN DIFFERENTIAL GIEMSA-STAINING OF SISTER CHROMATIDS [J]. CHROMOSOMA, 1978, 66 (04) : 351 - 359

[5] HERVA R, 1979, CLIN GENET, V17, P26

[6] BRDU-33258 HOECHST ANALYSIS OF DNA-REPLICATION IN HUMAN LYMPHOCYTES WITH SUPERNUMERARY OR STRUCTURALLY ABNORMAL X-CHROMOSOMES [J]. CHROMOSOMA, 1976, 57 (02) : 135 - 153

[7] DELETIONS OF CHROMOSOME-15 AS A CAUSE OF THE PRADER-WILLI SYNDROME [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1981, 304 (06) : 325 - 329

[8] RESOLUTION OF BREAKPOINTS IN A COMPLEX REARRANGEMENT BY USE OF MULTIPLE STAINING TECHNIQUES - CONFIRMATION OF SUSPECTED 12P12.3 INTRABAND BY DELETION DOSAGE EFFECT OF LDHB [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1981, 9 (02): : 95 - 103

[9] LYMPHOCYTE CHROMOSOME SURVEY IN 42 PATIENTS WITH RETINOBLASTOMA - EFFORT TO DETECT 13Q14 DELETION MOSAICISM [J]. HUMAN GENETICS, 1981, 58 (02) : 168 - 173

[10] THE ANIRIDIA-WILMS-TUMOR-ASSOCIATION - THE CRITICAL ROLE OF CHROMOSOME BAND 11P13 [J]. CANCER GENETICS AND CYTOGENETICS, 1980, 2 (02) : 131 - 137

[1] HIGH-RESOLUTION IN SITU HYBRIDIZATION TECHNIQUE FOR THE DIRECT VISUALIZATION OF LABELED G-BANDED EARLY METAPHASE AND PROPHASE CHROMOSOMES [J]. CYTOGENETICS AND CELL GENETICS, 1978, 22 (1-6): : 352 - 356

[2] ANIRIDIA-WILMS TUMOR ASSOCIATION - EVIDENCE FOR SPECIFIC DELETION OF 11P13 [J]. CYTOGENETICS AND CELL GENETICS, 1979, 24 (03): : 185 - 192

[3] FRANCKE U, 1977, CYTOGENET CELL GENET, V19, P107

[4] FACTORS INVOLVED IN DIFFERENTIAL GIEMSA-STAINING OF SISTER CHROMATIDS [J]. CHROMOSOMA, 1978, 66 (04) : 351 - 359

[5] HERVA R, 1979, CLIN GENET, V17, P26

[6] BRDU-33258 HOECHST ANALYSIS OF DNA-REPLICATION IN HUMAN LYMPHOCYTES WITH SUPERNUMERARY OR STRUCTURALLY ABNORMAL X-CHROMOSOMES [J]. CHROMOSOMA, 1976, 57 (02) : 135 - 153

[7] DELETIONS OF CHROMOSOME-15 AS A CAUSE OF THE PRADER-WILLI SYNDROME [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1981, 304 (06) : 325 - 329

[8] RESOLUTION OF BREAKPOINTS IN A COMPLEX REARRANGEMENT BY USE OF MULTIPLE STAINING TECHNIQUES - CONFIRMATION OF SUSPECTED 12P12.3 INTRABAND BY DELETION DOSAGE EFFECT OF LDHB [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 1981, 9 (02): : 95 - 103

[9] LYMPHOCYTE CHROMOSOME SURVEY IN 42 PATIENTS WITH RETINOBLASTOMA - EFFORT TO DETECT 13Q14 DELETION MOSAICISM [J]. HUMAN GENETICS, 1981, 58 (02) : 168 - 173

[10] THE ANIRIDIA-WILMS-TUMOR-ASSOCIATION - THE CRITICAL ROLE OF CHROMOSOME BAND 11P13 [J]. CANCER GENETICS AND CYTOGENETICS, 1980, 2 (02) : 131 - 137