Amanote Research
Register
Sign In
NPHP1 Gene Deletion Is a Rare Cause of Joubert Syndrome Related Disorders
Journal of Medical Genetics
- United Kingdom
doi 10.1136/jmg.2004.027375
Full Text
Open PDF
Abstract
Available in
full text
Categories
Genetics
Date
February 1, 2005
Authors
M Castori
Publisher
BMJ
Related search
Joubert Syndrome: A Rare Cause for Developmental Delay
Journal of Medical Science And clinical Research
Joubert Syndrome: A Rare Radiological Case
Cureus
The Diagnostic Utility of Exome Sequencing in Joubert Syndrome and Related Disorders
Journal of Human Genetics
Genetics
Mice With a Conditional Deletion of Talpid3 ( KIAA0586 ) – A Model for Joubert Syndrome
Journal of Pathology
Forensic Medicine
Pathology
Confirmation of EP300 Gene Mutations as a Rare Cause of Rubinstein–Taybi Syndrome
European Journal of Human Genetics
Genetics
A Rare Cause of Rhabdomyolysis: Gitelman Syndrome
International Journal of Case Reports and Images
Mounier Kuhn Syndrome Is Another Rare Cause for a Long Standing Dyspnea
Imaging in Medicine
Radiological
Radiology
Nuclear Medicine
Ultrasound Technology
Imaging
Aortic Aneurysm: A Rare Cause of Ortner’s Syndrome
Journal of Evolution of Medical and Dental Sciences
A Rare Cause of Difficult Intubation: Fraser Syndrome
Istanbul Medical Journal
