1.
Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene
by Jakkula, Eveliina
American journal of human genetics, 2010-02-12, Vol.86 (2), p.285-291
2.
Cohen Syndrome Is Caused by Mutations in a Novel Gene, COH1, Encoding a Transmembrane Protein with a Presumed Role in Vesicle-Mediated Sorting and Intracellular Protein Transport
by Kolehmainen, Juha
American journal of human genetics, 2003, Vol.72 (6), p.1359-1369
3.
Delineation of Cohen Syndrome Following a Large-Scale Genotype-Phenotype Screen
by Kolehmainen, Juha
American journal of human genetics, 2004, Vol.75 (1), p.122-127
Filter electronic articles 3 Hits
Remove Filters
- Journal Title
- The American Journal Of Human Ge... (3)
- American Journal Of Human Genetics
- Life Sciences & Biomedicine
- Medical Sciences (3)
- Humans (3)
- Genetics & Heredity (3)
- Genetics (3)
- General Aspects. Genetic Counseling (2)
- Female (2)
- Intellectual Disability - Genetics (2)
- Intellectual Disability - Pathology (2)
- Developmental Disabilities - Pat... (2)
- Male (2)
- Child (2)
- Abnormalities, Multiple - Genetics (2)
- Cohort Studies (2)
- Craniofacial Abnormalities - Gen... (2)
- Craniofacial Abnormalities - Pat... (2)
- Developmental Disabilities - Gen... (2)
- less ...