- VernacularTitle:微阵列比较基因组杂交在胎儿发育异常中的应用
 - Author:
	        		
		        		
		        		
			        		Lin WANG
			        		
			        		
			        		
			        			1
			        			,
			        		
			        			2
			        			
			        		
			        		
			        		
			        		
			        		;
		        		
		        		
		        		
			        		Xiaobin WANG
			        		
			        		;
		        		
		        		
		        		
			        		Na CAI
			        		
			        		;
		        		
		        		
		        		
			        		Bin HE
			        		
			        		;
		        		
		        		
		        		
			        		Qiuhua WU
			        		
			        		;
		        		
		        		
		        		
			        		Wei LI
			        		
			        		;
		        		
		        		
		        		
			        		Liping ZHANG
			        		
			        		;
		        		
		        		
		        		
			        		Xiaoping MA
			        		
			        		;
		        		
		        		
		        		
			        		Rong QIANG
			        		
			        		
		        		
		        		
		        		
			        		
			        		Author Information
			        		
 - Publication Type:Journal Article
 - MeSH: Adult; Chromosome Aberrations; Comparative Genomic Hybridization; methods; Congenital Abnormalities; genetics; DNA Copy Number Variations; Female; Humans; Pregnancy; Prenatal Diagnosis; methods
 - From: Chinese Journal of Medical Genetics 2017;34(5):691-694
 - CountryChina
 - Language:Chinese
 - 
		        	Abstract:
			       	
			       		
				        
				        	
OBJECTIVETo explore the genetic etiology for fetuses featuring intrauterine growth anomalies using array-based comparative genomic hybridization (aCGH).
METHODSForty-nine fetuses were enrolled in this study. Genomic DNA of the abortive tissues was analyzed with aCGH.
RESULTSFourteen (28.6%) samples were found with chromosomal aberrations, which included 8 chromosomal aneuploidies and 6 micro-aberrations (4 with known clinical pathogenecity and 2 with unknown clinical significance).
CONCLUSIONNumerical and structural chromosomal aberrations underlie a significant proportion of fetal growth anomalies. aCGH has provided an effective method for delineating their genetic cause.
 
            
