Zuffardi O, Fraccaro M
Hum Genet. 1982;62(3):280-1. doi: 10.1007/BF00333537.
The syndrome of torticollis, keloids, cryptorchidism and renal dysplasia was described by Goeminne (1968) in a large family, and listed as X-linked incomplete dominant by McKusick (1978; No. 31430). We mapped the locus on the long arm of the X chromosome at band q28 and distal to the G6PD locus. This was achieved by the chance discovery in the literature that two females, each with a balanced X/autosome translocation involving Xq28, had partial manifestation of the syndrome as was the case with the females in the larger family of Goeminne (1968).
戈明内(1968年)在一个大家庭中描述了斜颈、瘢痕疙瘩、隐睾症和肾发育不全综合征,并被麦库西克(1978年;第31430号)列为X连锁不完全显性遗传。我们将该基因座定位在X染色体长臂的q28带,且位于葡萄糖-6-磷酸脱氢酶(G6PD)基因座的远端。这是通过在文献中偶然发现两名女性实现的,她们各自有一个涉及Xq28的平衡X/常染色体易位,如同戈明内(1968年)较大的家族中的女性一样,有该综合征的部分表现。