18p1318:

Bojana Marković1,2, Marina Gazdić Janković3, Zoran Igrutinović1,2

  • 1Pediatric Clinic, University Clinical Centre Kragujevac, Zmaj Jovina 30, 34000 Kragujevac, Serbia.

PubMed
概括

单体性18p是一种罕见的染色体疾病,可以由13号和18号染色体之间的全臂转位引起. 这一案例突出显示了纹症是这种罕见遗传病的新型临床表现.

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