Raffel L J, Mohandas T, Rimoin D L
Am J Med Genet. 1986 Aug;24(4):607-11. doi: 10.1002/ajmg.1320240404.
We report a patient with the Killian/Teschler-Nicola/Pallister mosaic syndrome in association with a cytogenetic abnormality. This patient is the first reported to have lymphocyte mosaicism for an isochromosome of 12p. All other patients with the Killian syndrome have had normal lymphocyte karyotypes, although mosaicism for a similar isochromosome of 12p has been reported in the fibroblasts of most patients with the Killian syndrome.
我们报告了一例患有基利安/特施勒 - 尼古拉/帕利斯特嵌合综合征并伴有细胞遗传学异常的患者。该患者是首例被报道具有12号染色体短臂等臂染色体淋巴细胞嵌合现象的病例。所有其他患有基利安综合征的患者淋巴细胞核型均正常,不过大多数患有基利安综合征的患者成纤维细胞中已报道存在类似的12号染色体短臂等臂染色体嵌合现象。