Open Access Smith–Lemli–Opitz syndrome Journals

Smith–Lemli–Opitz syndrome is an inborn error of cholesterol synthesis. It is an autosomal recessive, multiple malformation syndrome caused by a mutation in the enzyme 7-Dehydrocholesterol reductase, or DHCR7.

All articles published in Open Access journals have undergone peer review and upon acceptance are immediately and permanently free for everyone to read and download.

This list of Smith–Lemli–Opitz syndrome OA journals will hopefully make it easier for you to have a better idea regarding where your want to publish your Smith–Lemli–Opitz syndrome manuscript.
Our list includes all the high-impact factor Smith–Lemli–Opitz syndrome journals that may be relevant to your field of study. In any case, we've also included other journals that may also offer more affordable publishing fees.We've made this extensive list of open access Smith–Lemli–Opitz syndrome journals so you can get a better overview of all the journals where you can publish open access.Use our different columns — number of papers, number of citations, and relevance — to find the best Smith–Lemli–Opitz syndrome venue for your manuscript.

The DOAJ columns refers to the The Directory of Open Access Journals, a list of open access journals, maintained by Infrastructure Services for Open Access.
There are certain criteria a journal must meet to be indexed by DOAJ, and thus inclusion in the DOAJ index is seen by scholars as a mark of quality.

All the open access Smith–Lemli–Opitz syndrome journals in this list are indexed in OA.mg.
If you spot any mistakes in this table of Smith–Lemli–Opitz syndrome OA journals, don’t hesitate to send us an email.