Related Experiment Videos
Genetic heterogeneity in metachromatic leukodystrophy
American Journal of Human Genetics
|March 1, 1982
Summary
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Function of Platelet-Induced Epithelial Attachment at Titanium Surfaces Inhibits Microbial Colonization.
Journal of dental research·2017
Structural alterations of the superior temporal gyrus in schizophrenia: Detailed subregional differences.
European psychiatry : the journal of the Association of European Psychiatrists·2016
Ultrasonographic findings in cubital tunnel syndrome caused by a cubitus varus deformity.
Hand surgery : an international journal devoted to hand and upper limb surgery and related research : journal of the Asia-Pacific Federation of Societies for Surgery of the Hand·2011
Neurodevelopmental abnormalities associated with severe congenital neutropenia due to the R86X mutation in the HAX1 gene.
Journal of medical genetics·2008
Activation and conformational changes of adenylate kinase in urea solution.
Science in China. Series C, Life sciences·2008
Variants leading to ELAVL2 haploinsufficiency cause a neurodevelopmental disorder with prominent cognitive, behavioral, and neurological features.
American journal of human genetics·2026
Cell villages and Dirichlet modeling map human cell fitness genetics.
American journal of human genetics·2026
Position effect at the SOX3 locus by an interchromosomal insertion causes hereditary spastic paraplegia.
American journal of human genetics·2026
Allele frequency trajectories across age groups reveal ongoing natural selection shaping disease susceptibility.
American journal of human genetics·2026
Transforming blood-derived episignatures into cell-type-agnostic classifiers: A shortcut to prenatal episignatures.
American journal of human genetics·2026
Additive value of polygenic risk and family history for coronary heart disease risk stratification in two diverse US cohorts.
American journal of human genetics·2026