Toncheva D, Genkova P, Tzoneva M, Lozanova T, Angelova E, Mitreva B
Acta Paediatr Hung. 1986;27(1):61-6.
High resolution analysis of the early metaphase and prometaphase chromosomes of the father of a child with malformations and mental retardation revealed inv dupl l(q21.4----q12). Almost the same was the aberration in the propositus but with a deletion of the band lq11.2 : 46,XX, inv dupl l(q21.4----q12)del lq11.2. This suggested that the malformations and mental retardation in the child were probably due to the microchromosome anomaly in the euchromatin, connected with the heterochromatin block in the father.
对一名患有畸形和智力迟钝儿童的父亲的早中期和前中期染色体进行高分辨率分析,发现存在inv dup 1(q21.4----q12)。先证者的畸变几乎相同,但缺失了1q11.2带:46,XX, inv dup 1(q21.4----q12)del 1q11.2。这表明该儿童的畸形和智力迟钝可能是由于常染色质中的微染色体异常,这与父亲的异染色质区有关。