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- [2] FISH characterization of small supernumerary marker chromosomes in two Prader-Willi patients AMERICAN JOURNAL OF MEDICAL GENETICS, 1997, 68 (01): : 99 - 104
- [3] Detection of chromosome 15 deletion in Prader-Willi syndrome using fluorescence in situ hybridization ARCHIVES OF ANDROLOGY, 2000, 45 (01): : 13 - 17
- [4] CASE OF PRADER-WILLI SYNDROME IN A GIRL WITH A SMALL EXTRA CHROMOSOME ACTA PAEDIATRICA SCANDINAVICA, 1971, 60 (02): : 222 - +
- [5] FLUORESCENT IN-SITU HYBRIDIZATION FOR DIAGNOSIS OF PRADER-WILLI ANGELMAN SYNDROME CYTOGENETICS AND CELL GENETICS, 1995, 69 (1-2): : 115 - 115
- [6] FLUORESCENT IN-SITU HYBRIDIZATION FOR EVALUATION OF PRADER-WILLI AND ANGELMAN SYNDROMES AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 57 (04): : 639 - 639
- [10] COMPARISON OF HIGH-RESOLUTION CHROMOSOME-BANDING AND FLUORESCENCE IN-SITU HYBRIDIZATION (FISH) FOR THE LABORATORY EVALUATION OF PRADER-WILLI-SYNDROME AND ANGELMAN SYNDROME AMERICAN JOURNAL OF MEDICAL GENETICS, 1994, 52 (01): : 85 - 91