Event ID : 10004 ( Case ID : 10527 ) |
| Patient Information: A three and a half year old girl |
| Symptom: Short stature, facial dysmorphism and developmental delay |
|
| Precision: C |
| Chromosome Rearrangement Type: Ring Chromosome |
| Karyotype : r(X)(p11.3q13) |
| First Breakpoint : |
| Second Breakpoint : |
| Involved Genes: NR_001564 |
| Junction Sequence is Unavailable . |
| Experimental Method: G Banding, FISH |
| PubMed ID: 11896455 |
| Authors: Tomkins DJ,McDonald HL,Farrell SA,Brown CJ |
| Journal: European journal of human genetics :
EJHG |
Go to Genome Browser ( Click the image ) |