Random triples
| Subject | Object |
|---|---|
| gptkb:cri_du_chat_syndrome | partial deletion of short arm of chromosome 5 |
| gptkb:de_la_Chapelle_syndrome | 46,XX karyotype |
| gptkb:20q13.2 | amplification |
| gptkb:46,XX_testicular_disorder_of_sex_development | 46,XX karyotype |
| gptkb:chromosome_11q23.1 | translocation t(9;11)(p22;q23) |
| gptkb:chromosome_11q23.1 | translocation t(4;11)(q21;q23) |
| gptkb:chromosome_11q23.1 | translocation t(11;19)(q23;p13.1) |