Related Experiment Videos
A modified method for prenatal diagnosis of Tay-Sachs disease in cell-free amniotic fluid
Monographs in Human Genetics
|January 1, 1978
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Two novel exonic point mutations in HEXA identified in a juvenile Tay-Sachs patient: role of alternative splicing and nonsense-mediated mRNA decay.
Molecular genetics and metabolism·2010
Neurocognitive testing in late-onset Tay-Sachs disease: a pilot study.
Journal of inherited metabolic disease·2008
Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish families.
Molecular psychiatry·2007
Is the WKL1 gene associated with schizophrenia?
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics·2004
31Phosphorus magnetic resonance spectroscopy in late-onset Tay-Sachs disease.
Journal of child neurology·2001
Injectable agents and hearing loss in the treatment of patients with rifampicin-resistant tuberculosis: a nationwide multicenter prospective study.
Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi·2026
Performance of In-Office Laryngeal Procedures Using Single-Use Endoscopes.
Journal of voice : official journal of the Voice Foundation·2026
Rapid and sensitive on-site detection of PBoV G3 using an EsCas13d-based platform.
Analytica chimica acta·2026