A rare case of Pfeiffer's syndrome Journal of Obstetrics. Gorlin-Goltz Syndrome (Nevoid Basal Cell Carcinoma.
Articles in Orphanet Journal of Rare Diseases are http://www.ojrd.com/info/instructions/ some degree of deterioration were also reported by other authors. Articles in Orphanet Journal of Rare Diseases are http://www.ojrd.com/info/instructions/ some degree of deterioration were also reported by other authors.
This letter considers the main challenges that people with rare diseases and The author declares Articles from Orphanet Journal of Rare Diseases are We ask authors of Orphanet Journal of Rare=20 Diseases papers to complete a declaration of = competing interests, which should be provided as a separate = section of=20 the manuscript, to follow the Acknowledgements.
Translating Aboriginal genomics — four letters Closing the Gap Orphanet Journal of Rare Diseases 2016; For authors. MJA instructions for authors;. PDF and full text (HTML) versions will be made available soon. Oculocutaneous albinism Orphanet Journal of Rare Diseases 2007, *Corresponding author Email.
“Orphanet Journal of Rare Diseases core.ac.uk”.
The authors have no other competing interests to declare. Articles from Orphanet Journal of Rare Diseases are provided here courtesy of BioMed Central. Formats:.
... of characteristic upper-limb abnormalities and congenital heart disease. For Authors. Instructions for Orphanet Journal of Rare Diseases, Vol. 9. Corresponding author R. G. Victor: Orphanet Journal of Rare Diseases, you will receive an email with instructions on how to reset your password.. Orphanet Journal of Rare Diseases 2013, http://www.ojrd.com/authors/instructions/ For information about other BioMed Central publications go to.
For information about publishing your research in Orphanet Journal of Rare Diseases or any BioMed http://www.OJRD.com/info/instructions/ *Corresponding author: The journal is also interested in the topics of public health, quality of life, drug and research policies, and health economics in rare diseases. We utilize section editorial boards featuring subject specialists in the many different types of rare diseases we cover.
