Skip to main content
Fig. 2 | Journal of Medical Case Reports

Fig. 2

From: Prenatal diagnosis of distal 13q deletion syndrome in a fetus with esophageal atresia: a case report and review of the literature

Fig. 2

Chromosomal analyses. a Results of Giemsa banding by amniocentesis. The arrow indicates the abnormal chromosome 13, as del(13)(q32.1). b The result of fluorescent in situ hybridization by amniocentesis. The normal chromosome 13 had both 13q14 (blue) and 13qter (yellow), but no signal indicative of 13qter was detected on the chromosome del(13)(q32.1). c Array CGH analysis reveals the deleted region of 13q31.2–qter (92973314–115097664). The right panel shows an enlarged view of the gene deletion site in the left panel

Back to article page

Journal of Medical Case Reports

ISSN: 1752-1947