Fibrodysplasia Ossificans Progressiva: Clinical Course, Genetic Mutations and Genotype-Phenotype Correlation

Publisher： Karger

E-ISSN： 1661-8777|5|5|201-211

ISSN： 1661-8769

Source： Molecular Syndromology, Vol.5, Iss.5, 2014-08, pp. : 201-211

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

Atypical fibrodysplasia ossificans progressiva diagnosed by whole‐exome sequencing

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 6, 2015-06 ,pp. : 1337-1341

John Wiley & Sons Inc

Access to resources Recommend Favorite

Spectrum of FOXL2 gene mutations in blepharophimosis-ptosis-epicanthus inversus (BPES) families demonstrates a genotype–phenotype correlation

By Maldergem L.V.  

Human Molecular Genetics, Vol. 10, Iss. 15, 2001-07 ,pp. : 1591-1600

Oxford University Press

Access to resources Recommend Favorite

Functional analysis of mutations in SLC7A9 , and genotype–phenotype correlation in non-Type I cystinuria

By Bisceglia L.  

Human Molecular Genetics, Vol. 10, Iss. 4, 2001-02 ,pp. : 305-316

Oxford University Press

Access to resources Recommend Favorite

Genotype–phenotype correlation in inherited severe insulin resistance

By Longo N.  

Human Molecular Genetics, Vol. 11, Iss. 12, 2002-06 ,pp. : 1465-1475

Oxford University Press

Access to resources Recommend Favorite

Genotype–phenotype correlation in von Hippel-Lindau syndrome

By A.Friedrich C.  

Human Molecular Genetics, Vol. 10, Iss. 7, 2001-04 ,pp. : 763-767

Oxford University Press

Access to resources Recommend Favorite