Menko F H, Madan K, Baart J A, Beukenhorst H L
Department of Clinical Genetics, Free University Hospital, Amsterdam, The Netherlands.
Am J Med Genet. 1992 Nov 15;44(5):696-8. doi: 10.1002/ajmg.1320440532.
We have investigated a patient with the Robin sequence and a unilateral deficiency of the left forearm. She was found to have a terminal deletion of the long arm of chromosome 4, del(4)(q33). The clinical manifestations of this patient differ from those of 7 previously described patients with a deletion of the same segment.
我们研究了一名患有罗宾序列征和左侧前臂单侧缺失的患者。发现她存在4号染色体长臂末端缺失,即del(4)(q33)。该患者的临床表现与之前描述的7名具有相同片段缺失的患者不同。