Event ID : 10690 ( Case ID : 12269 ) |
| Symptom: Microcephaly, epicanthal folds, midface hypoplasia, and abnormally modeled ears, hearing loss |
|
| Precision: C |
| Chromosome Rearrangement Type: Inversion |
| Karyotype : inv(18)(q21.1q23) |
| First Breakpoint : |
| Second Breakpoint : |
| Junction Sequence is Unavailable . |
| Experimental Method: FISH, PCR |
| PubMed ID: 9556294 |
| Authors: Keppler-Noreuil KM,Carroll
AJ,Finley SC,Descartes M,Cody JD,DuPont BR,Gay CT,Leach RJ |
| Journal: American journal of medical
genetics |
Go to Genome Browser ( Click the image ) |