8 results on '"Gofin, Yoel"'
Search Results
2. Bi-allelic variants in CEP295 cause Seckel-like syndrome presenting with primary microcephaly, developmental delay, intellectual disability, short stature, craniofacial and digital abnormalities
3. Expanded Clinical Phenotype and Untargeted Metabolomics Analysis in RARS2-related Mitochondrial Disorder (P2-8.003)
4. Expanded clinical phenotype and untargeted metabolomics analysis in RARS2-related mitochondrial disorder: a case report
5. A familial deletion of 10p12.1 associated with thrombocytopenia.
6. P792: Amniotic fluid fetal DNA concentration is higher in females and varies with gestational age
7. P560: Community-oriented genetics: Establishing a new pediatric genetics clinic in the Muslim-Arab City of Tayibe, Israel
8. Two versus one newborn screens: Policy considerations for state newborn screening laboratories based on the Texas experience.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.