Publisher: John Wiley & Sons Inc
E-ISSN: 1098-1004|36|2|232-239
ISSN: 1059-7794
Source: HUMAN MUTATION, Vol.36, Iss.2, 2015-02, pp. : 232-239
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
A study of 133 Chinese children with mitochondrial respiratory chain complex I deficiency
CLINICAL GENETICS, Vol. 87, Iss. 2, 2015-02 ,pp. :
DLL4 loss‐of‐function heterozygous mutations cause Adams–Oliver syndrome
CLINICAL GENETICS, Vol. 88, Iss. 6, 2015-12 ,pp. :
FERMT1 promoter mutations in patients with Kindler syndrome
CLINICAL GENETICS, Vol. 88, Iss. 3, 2015-09 ,pp. :