Related Experiment Videos
The genetics of the spinal muscular atrophies
1Hospital for Sick Children, London, U.K.
Progress in Clinical and Biological Research
|January 1, 1989
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Natural history, symptoms and treatment of the narcoleptic syndrome.
Acta neurologica Scandinavica·2009
Evidence for digenic inheritance in some cases of Antley-Bixler syndrome?
Journal of medical genetics·2000
Rapadilino syndrome--a non-Finnish case.
Clinical dysmorphology·1998
Three patients with the osteochondrodysplasia and hypertrichosis syndrome--Cantu syndrome.
Clinical dysmorphology·1998
DNA homology and chromosome stability: a sensitive yeast genetic system for identifying double-stranded DNA damage.
Progress in clinical and biological research·2018
Interaction of lipopolysaccharide with a mammalian lyso-phosphatidate acyltransferase (LPAAT) transfected into E. coli, and effect of lisofylline on LPAAT transfected into mammalian cells.
Progress in clinical and biological research·1998
The molecular basis for therapeutic concepts utilizing CD14.
Progress in clinical and biological research·1998
Endotoxin tolerance alters macrophage membrane regulatory G proteins.
Progress in clinical and biological research·1998
Molecular mechanisms responsible for endotoxin tolerance.
Progress in clinical and biological research·1998
Antibiotic-mediated release of endotoxin and the pathogenesis of gram-negative sepsis.
Progress in clinical and biological research·1998
Network analysis of the genetic relationships between twenty psychiatric and substance use disorders.
World psychiatry : official journal of the World Psychiatric Association (WPA)·2026
Clinical Utility of Trio Exome Sequencing in Rwandan Children With Autism Spectrum Disorder.
Molecular genetics & genomic medicine·2026
Large-Scale Neuroimaging and Genetic Analyses of the Human Thalamus in Loneliness.
Biological psychiatry global open science·2026
A recurrent CCDC82 frameshift variant associated with syndromic neurodevelopmental disorder in a consanguineous Pakistani family.
Biochemistry and biophysics reports·2026