Tabor A, Andersen O, Lundsteen C, Niebuhr E, Sardemann H
Hum Genet. 1983;64(2):196-9. doi: 10.1007/BF00327127.
A family in which an intestitial deletion of the X chromosome, del(X)(q13q21.3), is segregating was ascertained through a boy with cleft lip and palate, agenesis of the corpus callosum, and severe mental retardation. The possible causal relationship to his chromosome abnormality is discussed. Although the deletion occurred within the critical region, the mother showed no signs of gonadal dysgenesis. A phenotypically normal daughter was, as her mother, monosomic for this region of the X, and both showed random inactivation of the X chromosome.
通过一名患有唇腭裂、胼胝体发育不全和严重智力迟钝的男孩,确定了一个X染色体间质缺失del(X)(q13q21.3)正在进行分离的家族。讨论了其与染色体异常可能的因果关系。虽然缺失发生在关键区域内,但母亲没有性腺发育不全的迹象。一个表型正常的女儿与其母亲一样,在X染色体的这个区域是单体型,并且两者都表现出X染色体的随机失活。