Related Experiment Videos
Letter: Genetic heterogeneity in fucosidosis
Lancet (London, England)
|December 15, 1973
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Structural brain anomalies in Cri-du-Chat syndrome: MRI findings in 14 patients and possible genotype-phenotype correlations.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society·2020
Late-onset Pompe disease: a genetic-radiological correlation on cerebral vascular anomalies.
Journal of neurology·2017
Nasal powders of thalidomide for local treatment of nose bleeding in persons affected by hereditary hemorrhagic telangiectasia.
International journal of pharmaceutics·2016
Radiosensitivity in lymphoblastoid cell lines derived from Shwachman-Diamond syndrome patients.
Radiation protection dosimetry·2015
LOPED study: looking for an early diagnosis in a late-onset Pompe disease high-risk population.
Journal of neurology, neurosurgery, and psychiatry·2015
Cardiovascular disease in pregnancy: physiology, global burden, risk stratification, and opportunities in care.
Lancet (London, England)·2026
Adverse pregnancy outcomes and long-term cardiovascular disease risk.
Lancet (London, England)·2026
Altered Hepatic Gene Expression under Choline-Deficient Conditions.
Journal of nutritional science and vitaminology·2026
Distal Radius Morphology and Bone Mineral Density Show Significant Sex- and Age-Based Differences With Implications for Allograft Glenoid Reconstruction.
Arthroscopy : the journal of arthroscopic & related surgery : official publication of the Arthroscopy Association of North America and the International Arthroscopy Association·2026
Haplotype-based association of HTR2A rs6311-rs6313 with early risperidone-clozapine response in Batak patients with schizophrenia.
Pharmacogenetics and genomics·2026