Related Experiment Videos
A case report of Teschler-Nicola/Killian syndrome
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Nine novel mutations in NR0B1 (DAX1) causing adrenal hypoplasia congenita.
Human mutation·2001
Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21.
American journal of human genetics·1989
Familial Prader-Willi syndrome with apparently normal chromosomes.
American journal of medical genetics·1987
Chronic renal failure and XY gonadal dysgenesis: "Frasier" syndrome--a commentary on reported cases.
American journal of medical genetics. Supplement·1987
VATER and other associations: historical perspectives and modern interpretations.
American journal of medical genetics. Supplement·1986
Syndrome of amelogenesis imperfecta, nephrocalcinosis, impaired renal concentration, and possible abnormality of calcium metabolism.
American journal of medical genetics·1985
Machine-Vision-Authenticated Hue-Programmable Bilayer Heterostructures for Anticounterfeiting.
ACS applied materials & interfaces·2026
Sub-stoichiometric 5-methoxyuridine modification enables tunable immune evasion and protein expression from synthetic mRNAs.
Molecular therapy. Nucleic acids·2026
Size-dependent surface engineering of magnetic micro/nanorobots for synergistic chemo-magnetothermal cancer therapy.
Chemical communications (Cambridge, England)·2026