Related Experiment Videos
Discriminant function of dermatoglyphic patterns of Down's syndrome
Summary
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Protective effect of UDCA against IL-11- induced cardiac fibrosis is mediated by TGR5 signalling.
Frontiers in cardiovascular medicine·2024
Deshima 2.0: Rapid Redshift Surveys and Multi-line Spectroscopy of Dusty Galaxies.
Journal of low temperature physics·2022
Are fructophilic lactic acid bacteria (FLAB) beneficial to humans?
Beneficial microbes·2022
Age and geographic dependence of Zika virus infection during the outbreak on Yap island, 2007.
Mathematical biosciences and engineering : MBE·2020
Bias correction methods for test-negative designs in the presence of misclassification.
Epidemiology and infection·2020
Gene-deletion and carrier detections, and prenatal diagnosis of Duchenne muscular dystrophy by analysis of the dystrophin gene amplified by polymerase chain reaction.
Jinrui idengaku zasshi. The Japanese journal of human genetics·1991
Rapid detection of a point mutation in thyroid-stimulating hormone beta-subunit gene causing congenital isolated thyroid-stimulating hormone deficiency.
Jinrui idengaku zasshi. The Japanese journal of human genetics·1991
Biochemical characteristics of glucose-6-phosphate dehydrogenase variants among the Malays of Singapore with report of a new non-deficient (GdSingapore) and three deficient variants.
Jinrui idengaku zasshi. The Japanese journal of human genetics·1991
Similar proportion of sporadic cases in cytochrome b558 negative chronic granulomatous disease and Duchenne muscular dystrophy.
Jinrui idengaku zasshi. The Japanese journal of human genetics·1991
The MspI restriction fragment length polymorphism of human aldolase B gene on chromosome 9q21.3-q22.2.
Jinrui idengaku zasshi. The Japanese journal of human genetics·1991
The prevalence at birth of cogenital malformations at a maternity hospital in Osaka City, 1948-1990.
Jinrui idengaku zasshi. The Japanese journal of human genetics·1991
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