作者: J. Kučera , P. Goetz
DOI: 10.1007/BF00446414
关键词: Biology 、 Pediatrics 、 Human genetics
摘要: Four consecutively born siblings were affected by Exomphalos. In 2 cases, major and minor anomalies associated. Cytogenetic examination of the fourth infant revealed a normal karyogram. The parents their families did not exhibit any relevant genetic defect. On other hand it is unlikely that such series exomphalos was due to chance.