Use my Search Websuite to scan PubMed, PMCentral, Journal Hosts and Journal Archives, FullText. Kick-your-searchterm to multiple Engines kick-your-query now !>

A dictionary by aggregated review articles of nephrology, medicine and the life sciences Your one-stop-run pathway from word to the immediate pdf of peer-reviewed on-topic knowledge.

10.1155/2016/9790169 http://scihub22266oqcxt.onion/10.1155/2016/9790169 C4749774!4749774!26942024     free     free     free Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 217.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Case+Rep+Genet 2016 ; 2016 (ä): ä Nephropedia Template TP {{tp|p=26942024|t=2016. Angelman-Like Syndrome: A Genetic Approach to Diagnosis with Illustrative Cases |pdf=|usr=}}{{26942024}} gab.com Text Angelman-Like Syndrome: A Genetic Approach to Diagnosis with Illustrative Cases JO: Case Rep Genet http://www.kidney.de/pget.php?&tw=1&pmid=26942024 #FOAvip Epigenetic abnormalities in 15q11-13 imprinted region and UBE3A mutation are the two major mechanisms for molecularly confirmed Angelman Syndrome. However, there is 10% of clinically diagnosed Angelman Syndrome remaining test negative. With the advancement of genomic technology like array comparative genomic hybridization and next generation sequencing methods, it is found that some patients of these test negative Angelman-like Syndromes actually have alternative diagnoses. Accurate molecular diagnosis is paramount for genetic counseling and subsequent management. Despite overlapping phenotypes between Angelman and Angelman-like Syndrome, there are some subtle but distinct features which could differentiate them clinically. It would provide important clue during the diagnostic process for clinicians. Twit Text FOAVip Angelman-Like Syndrome: A Genetic Approach to Diagnosis with Illustrative Cases ????Case Rep Genet http://www.kidney.de/pget.php?&tw=1&pmid=26942024 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26942024 #FOAvip English Wikipedia <ref>{{Cite pmid|26942024}}</ref> Angelman-Like Syndrome: A Genetic Approach to Diagnosis with Illustrative Cases #MMPMID26942024 Luk HM Case Rep Genet 2016[]; 2016 (ä): ä PMID26942024show ga Epigenetic abnormalities in 15q11-13 imprinted region and UBE3A mutation are the two major mechanisms for molecularly confirmed Angelman Syndrome. However, there is 10% of clinically diagnosed Angelman Syndrome remaining test negative. With the advancement of genomic technology like array comparative genomic hybridization and next generation sequencing methods, it is found that some patients of these test negative Angelman-like Syndromes actually have alternative diagnoses. Accurate molecular diagnosis is paramount for genetic counseling and subsequent management. Despite overlapping phenotypes between Angelman and Angelman-like Syndrome, there are some subtle but distinct features which could differentiate them clinically. It would provide important clue during the diagnostic process for clinicians. äAngelman-Like Syndrome: A Genetic Approach to Diagnosis with Illustrat(epmc).pdf DeepDyve Pubget Overpricing