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10.1053/j.semperi.2014.10.009 http://scihub22266oqcxt.onion/10.1053/j.semperi.2014.10.009 C4883661!4883661!25444417     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=25444417&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\25444417.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Semin+Perinatol 2015 ; 39 (1): 44-54 Nephropedia Template TP {{tp|p=25444417|t=2015. Recent advances of genomic testing in perinatal medicine |pdf=|usr=}}{{25444417}} gab.com Text Recent advances of genomic testing in perinatal medicine JO: Semin Perinatol http://www.kidney.de/pget.php?&tw=1&pmid=25444417 #FOAvip Rapid progress in genomic medicine in recent years has made it possible to diagnose subtle genetic abnormalities in a clinical setting on routine basis. This has allowed for detailed genotype-phenotype correlations and the identification of the genetic basis of many congenital anomalies. In addition to the availability of chromosomal microarray analysis, exome and whole genome sequencing on pre- and postnatal samples of cell free DNA has revolutionized the field of prenatal diagnosis. Incorporation of these technologies in perinatal pathology is bound to play a major role in coming years. In this communication, we briefly present the current experience with use of classical chromosome analysis, fluorescence in situ hybridization, and microarray testing, development of whole genome analysis by next generation sequencing technology, offer a detailed review of the history and current status of noninvasive prenatal testing using cell free DNA, and discuss the advents of these new genomic technologies in perinatal medicine. Twit Text FOAVip Recent advances of genomic testing in perinatal medicine ????Semin Perinatol http://www.kidney.de/pget.php?&tw=1&pmid=25444417 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=25444417 #FOAvip English Wikipedia <ref>{{Cite pmid|25444417}}</ref> Recent advances of genomic testing in perinatal medicine #MMPMID25444417 Peters DG; Yatsenko SA; Surti U; Rajkovic A Semin Perinatol 2015[Feb]; 39 (1): 44-54 PMID25444417show ga Rapid progress in genomic medicine in recent years has made it possible to diagnose subtle genetic abnormalities in a clinical setting on routine basis. This has allowed for detailed genotype-phenotype correlations and the identification of the genetic basis of many congenital anomalies. In addition to the availability of chromosomal microarray analysis, exome and whole genome sequencing on pre- and postnatal samples of cell free DNA has revolutionized the field of prenatal diagnosis. Incorporation of these technologies in perinatal pathology is bound to play a major role in coming years. In this communication, we briefly present the current experience with use of classical chromosome analysis, fluorescence in situ hybridization, and microarray testing, development of whole genome analysis by next generation sequencing technology, offer a detailed review of the history and current status of noninvasive prenatal testing using cell free DNA, and discuss the advents of these new genomic technologies in perinatal medicine. äRecent advances of genomic testing in perinatal medicine (epmc).pdf DeepDyve Pubget Overpricing