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["Type","Disease","Fail","Success"]
["Micro deletion &    Duplication","ALAGILLE SYNDROME",0,1]
[null,"ANGELMAN SYNDROME",0,1]
[null,"CRI-DU-CHAT SYNDROME",0,10]
[null,"DIGEORGE SYNDROME",0,14]
[null,"GLYCEROL KINASE DEFICIENCY",0,1]
[null,"KALLMANN SYNDROME 1",0,0]
[null,"MILLER-DIEKER LISSENCEPHALY SYNDROME",0,2]
[null,"MONOSOMY 1p36 SYNDROME",0,0]
[null,"MUSCULAR DYSTROPHY, DUCHENNE TYPE",0,1]
[null,"NEUROFIBROMATOSIS, TYPE I",0,1]
[null,"NEUROFIBROMATOSIS, TYPE II",0,1]
[null,"PRADER-WILLI SYNDROME",0,33]
[null,"SEX-DETERMINING REGION Y",0,0]
[null,"SMITH-MAGENIS SYNDROME",0,2]
[null,"SOTOS SYNDROME",0,0]
[null,"SPERMATOGENIC FAILURE, NONOBSTRUCTIVE, Y-LINKED",0,1]
[null,"STEROID SULFATASE DEFICIENCY DISEASE",0,1]
[null,"WILLIAMS-BEUREN SYNDROME",0,3]
[null,"WOLF-HIRSCHHORN SYNDROME",0,2]
["Aneuploidy    ","Trisomy 13",0,19]
[null,"Trisomy 18",0,24]
[null,"Trisomy 21",0,10]
[null,"Turner syndrome (45,X)",0,1]
[null,"Klinefelter syndrome (47,XXY)",0,2]
[null,"Triple X (47,XXX)",0,1]
[null,"47,XYY",0,1]
[{"$nulls":3},132]

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