核型
染色体易位
SNP阵列
荧光原位杂交
生物
遗传学
SNP公司
单核苷酸多态性
染色体
比较基因组杂交
基因型
基因
作者
Na Ma,Jialun Pang,Ying Peng,Zhengjun Jia,Hui Xi,Guoying Liu,Yuchun Zhou,Hua Wang
出处
期刊:PubMed
日期:2019-12-10
卷期号:36 (12): 1199-1202
标识
DOI:10.3760/cma.j.issn.1003-9406.2019.12.012
摘要
To carry out genetic testing for a boy presenting with mental retardation and hypoplasia.Conventional karyotyping, fluorescence in situ hybridization (FISH) and single nucleotide polymorphism based array (SNP-array) were used to analyze the boy and his parents.SNP-array has detected a 25.7 Mb microduplication at 2q33.3q36.3 in the boy. Chromosomal karyotyping and FISH analysis indicated that his mother had a karyotype of 46,XX,ish ins(11;2) (p15;q33q36), and that the boy has carried an abnormal chromosome 11 derived from the maternal translocation. The karyotype of the boy was ascertained as 46,XY,ish der(11)ins(11;2) (p15;q33q36)mat.SNP-array combined with G-banding and FISH can delineate the cryptic translocation and is valuable for the assessment of recurrence risk for subsequent pregnancies.
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