Related Experiment Videos
Molecular dysmorphology: an approach to Down's syndrome
Annals of the New York Academy of Sciences
|January 1, 1986
Summary
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Recombination-based assay (RBA) for screening bacteriophage lambda libraries.
Current protocols in molecular biology·2008
Sensitive detection of human papillomavirus in cervical, head/neck, and schistosomiasis-associated bladder malignancies.
Proceedings of the National Academy of Sciences of the United States of America·2005
Rap1, a small GTP-binding protein is upregulated during arrest of proliferation in human keratinocytes.
Journal of cellular physiology·2003
Cerium Alloying in Nanobainitic Steel: A Double-Edged Effect on Austenite and Toughness.
Annals of the New York Academy of Sciences·2026
Landscape Preferences and Leisure Constraints in Age-Friendly Community Parks.
Annals of the New York Academy of Sciences·2026
Toward Meta-Omics Governance of the Urban Microbiome Commons.
Annals of the New York Academy of Sciences·2026
Rhythmic Structure Shapes Dyadic Self-Other Representations Through Interpersonal Action Coupling.
Annals of the New York Academy of Sciences·2026
On the Limitations of Burnout as an Indicator of Job-Related Distress.
Annals of the New York Academy of Sciences·2026
First Records of Ixodes ventalloi and Ixodes frontalis on Vegetation in Tunisia: Bird-Mediated Dispersal Scenario?
Annals of the New York Academy of Sciences·2026
Crystal structure of the NKX2-1 homeodomain bound to a palindromic DNA recognition sequence.
Acta crystallographica. Section F, Structural biology communications·2026
EXTL3 dysfunction identified as a driver of aberrant bone development in severe familial ankylosing spondylitis.
Annals of the rheumatic diseases·2026
Dopamine Receptor D2 gene Polymorphisms rs2005313, rs4274224, and rs4938019 in Pakistani Patients with Schizophrenia:a Diagnostic Tool for Schizophrenia.
Journal of molecular neuroscience : MN·2026
Approach to The Patient With Combined Pituitary Hormone Deficiency Due to a Novel Homozygous LHX3 Variant.
Clinical endocrinology·2026
CCDC149: a novel gene associated with hypopituitarism and neurodevelopmental impairment.
European journal of endocrinology·2026