Cheng E Y, Chen Y J, Disteche C M, Gartler S M
Department of Obstetrics and Gynecology, University of Washington Medical Center, Seattle 98195-6460, USA.
Hum Genet. 1999 Sep;105(3):191-6. doi: 10.1007/s004399900120.
A cytological analysis of the pairing configurations in meiosis in a 19-week human fetus with a de novo paracentric inversion of chromosome 7 (q11.23)(q21.1) is reported, using fluorescent in situ hybridization with a chromosome 7 DNA library, a DNA probe for the centromeric region of chromosome 7, and a probe for the William Syndrome Critical Region (WSCR) at 7q11.23. Of 1079 pachytene cells, 58% exhibited complete heterosynapsis of the inverted region while only 10.3% of cells exhibited the expected loop formation. Meiotic progression was observed to be normal.
报道了对一名19周龄人类胎儿减数分裂中配对构型的细胞学分析,该胎儿染色体7发生了新发的臂内倒位(q11.23)(q21.1)。使用7号染色体DNA文库、7号染色体着丝粒区域的DNA探针以及7q11.23处威廉姆斯综合征关键区域(WSCR)的探针进行荧光原位杂交。在1079个粗线期细胞中,58%的细胞在倒位区域表现出完全异源联会,而只有10.3%的细胞表现出预期的环形成。观察到减数分裂进程正常。