![](/images/ico/ico_close.png)
![](/images/ico/ico5.png)
Publisher: John Wiley & Sons Inc
E-ISSN: 1399-0004|87|6|533-534
ISSN: 0009-9163
Source: CLINICAL GENETICS, Vol.87, Iss.6, 2015-06, pp. : 533-534
Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.
Abstract
Related content
![](/images/ico/ico_close.png)
![](/images/ico/ico5.png)
Mismatch repair genes founder mutations and cancer susceptibility in Lynch syndrome
CLINICAL GENETICS, Vol. 87, Iss. 6, 2015-06 ,pp. :
![](/images/ico/ico_close.png)
![](/images/ico/ico5.png)
Mutations in FLVCR2 associated with Fowler syndrome and survival beyond infancy
CLINICAL GENETICS, Vol. 89, Iss. 1, 2016-01 ,pp. :
![](/images/ico/ico_close.png)
![](/images/ico/ico5.png)
POLD1 Germline Mutations in Patients Initially Diagnosed with Werner Syndrome
HUMAN MUTATION, Vol. 36, Iss. 11, 2015-11 ,pp. :
![](/images/ico/ico_close.png)
![](/images/ico/ico5.png)
Molecular Diversity and Associated Phenotypic Spectrum of Germline CBL Mutations
HUMAN MUTATION, Vol. 36, Iss. 8, 2015-08 ,pp. :
![](/images/ico/ico_close.png)
![](/images/ico/ico5.png)
Detection of novel germline mutations for breast cancer in non‐BRCA1/2 families
FEBS JOURNAL (ELECTRONIC), Vol. 282, Iss. 17, 2015-09 ,pp. :