17Q INVERSION INVOLVING THE NEUROFIBROMATOSIS TYPE ONE LOCUS IN A FAMILY WITH NEUROFIBROMATOSIS TYPE ONE

被引:4
作者
ASAMOAH, A
NORTH, K
DORAN, S
WAGSTAFF, J
OGLE, R
COLLINS, FS
KORF, BR
机构
[1] CHILDRENS HOSP,DIV GENET,BOSTON,MA 02115
[2] CHILDRENS HOSP,DEPT GENET,SYDNEY,NSW,AUSTRALIA
[3] NATL CTR HUMAN GENOME RES,ANN ARBOR,MI
[4] UNIV MICHIGAN,ANN ARBOR,MI 48109
来源
AMERICAN JOURNAL OF MEDICAL GENETICS | 1995年 / 60卷 / 04期
关键词
PARACENTRIC INVERSION; CHROMOSOMES; FLUORESCENCE IN SITU HYBRIDIZATION; FIELD INVERSION GEL ELECTROPHORESIS; MUTATION;
D O I
10.1002/ajmg.1320600410
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We report a family with a paracentric inversion of the long arm of chromosome 17 [inv(17)(q11.2q25.1)] and neurofibromatosis type one (NF1), The family was ascertained because of NF1 and multiple miscarriages. Fluorescence in situ hybridization using cosmid probes from opposite ends of the NF1 gene confirmed that the inversion disrupts the gene, Using field inversion gel electrophoresis we have found that the inversion separates cDNA probes FB5D and AE25, which are normally adjacent to one another in the NF1 gene. This is the third published report of a gross chromosomal rearrangement responsible for NF1, The features in this family are typical for NF1, and are not unusually severe. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:312 / 316
页数:5
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