DETECTION BY FLUORESCENCE IN-SITU HYBRIDIZATION OF CHROMOSOME-4, CHROMOSOME-6, CHROMOSOME-7, CHROMOSOME-8, CHROMOSOME-9, CHROMOSOME-10, CHROMOSOME-11, CHROMOSOME-12, CHROMOSOME-13, CHROMOSOME-17, CHROMOSOME-18, CHROMOSOME-21, CHROMOSOME-X AND CHROMOSOME-Y ANEUPLOIDY IN SPERM FROM OLIGO-ASTHENO-TERATO-ZOOSPERMIC PATIENTS OF AN IN-VITRO FERTILIZATION PROGRAM
Mg. Pang et al., DETECTION BY FLUORESCENCE IN-SITU HYBRIDIZATION OF CHROMOSOME-4, CHROMOSOME-6, CHROMOSOME-7, CHROMOSOME-8, CHROMOSOME-9, CHROMOSOME-10, CHROMOSOME-11, CHROMOSOME-12, CHROMOSOME-13, CHROMOSOME-17, CHROMOSOME-18, CHROMOSOME-21, CHROMOSOME-X AND CHROMOSOME-Y ANEUPLOIDY IN SPERM FROM OLIGO-ASTHENO-TERATO-ZOOSPERMIC PATIENTS OF AN IN-VITRO FERTILIZATION PROGRAM, American journal of human genetics, 57(4), 1995, pp. 680-680