The clinical utility of whole‐exome sequencing in the context of rare diseases – the changing tides of medical practice

Publisher： John Wiley & Sons Inc

E-ISSN： 1399-0004|9-9163|4|313-319

ISSN： 0009-9163

Source： CLINICAL GENETICS, Vol.9-9163, Iss.4, 2015-10, pp. : 313-319

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

The clinical utility of whole‐exome sequencing in the context of rare diseases – the changing tides of medical practice

By  

CLINICAL GENETICS, Vol. 88, Iss. 4, 2015-10 ,pp. : 313-319

John Wiley & Sons Inc

Access to resources Recommend Favorite

Whole‐exome sequencing broadens the phenotypic spectrum of rare pediatric epilepsy: a retrospective study

By  

CLINICAL GENETICS, Vol. 88, Iss. 1, 2015-07 ,pp. : 34-40

John Wiley & Sons Inc

Access to resources Recommend Favorite

Whole‐exome targeted sequencing of the uncharacterized pine genome

By  

THE PLANT JOURNAL, Vol. 75, Iss. 1, 2013-07 ,pp. : 146-156

John Wiley & Sons Inc

Access to resources Recommend Favorite

Resolving clinical diagnoses for syndromic cleft lip and/or palate phenotypes using whole‐exome sequencing

By  

CLINICAL GENETICS, Vol. 9-9163, Iss. 5, 2015-11 ,pp. : 441-449

John Wiley & Sons Inc

Access to resources Recommend Favorite

Resolving clinical diagnoses for syndromic cleft lip and/or palate phenotypes using whole‐exome sequencing

By  

CLINICAL GENETICS, Vol. 88, Iss. 5, 2015-11 ,pp. : 441-449

John Wiley & Sons Inc

Access to resources Recommend Favorite