Search filters

Authors whose works are in public domain in at least one jurisdiction

List of works by Paul Rutland

A novel homeobox mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome associated with brain, ocular, and dental phenotypes.

scientific article published in March 2006

FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy

scientific article

FOXRED1, encoding an FAD-dependent oxidoreductase complex-I-specific molecular chaperone, is mutated in infantile-onset mitochondrial encephalopathy

scientific article published on 28 May 2015

First report of Mycobacterium bovis DNA in human remains from the Iron Age.

scientific article

Frameshift mutation in GJA12 leading to nystagmus, spastic ataxia and CNS dys-/demyelination

scientific article

Fraser syndrome and mouse blebbed phenotype caused by mutations in FRAS1/Fras1 encoding a putative extracellular matrix protein

scientific article

Genomic Insights into Cardiomyopathies: A Comparative Cross-Species Review

scientific article published on 21 March 2017

Kantaputra mesomelic dysplasia: a second reported family

scientific article published in July 2004

Mitochondrial m.1584A 12S m62A rRNA methylation in families with m.1555A>G associated hearing loss

scientific article published on 09 October 2014

Mycobacterium leprae genotype amplified from an archaeological case of lepromatous leprosy in Central Asia

article

Paulina is supported by:

About Paulina

Help