Results 41 to 50 of about 4,415 (205)

Soles dermatoglyphics in the prognosis of sport endowments: forming of soles dermatoglyphics in the Ukrainian population (information 1) [PDF]

open access: yesPedagogìka, Psihologìâ ta Mediko-bìologìčnì Problemi Fìzičnogo Vihovannâ ì Sportu, 2013
Comparative indexes are considered for determination of dermatoglyphic markers feet in relation to a sporting gift. In an experiment took part 209 youths and 198 girls in age 17-19 years.
Serhiyenko L.P., Lyshevska V.M.
doaj   +3 more sources

Acral Melanocytic Lesions Under Conventional, Sub‐Ultraviolet Reflectance, and Ultraviolet‐Induced Fluorescence Dermoscopy: A Comparative Analysis

open access: yesInternational Journal of Dermatology, EarlyView.
Conventional dermoscopy provided higher scores than ultraviolet‐induced fluorescence dermoscopy for parallel furrow pattern, parallel ridge pattern (PRP), fibrillar pattern, dots/clods, radial lines, blue–white structureless areas and blotch, and outperformed sub‐ultraviolet reflectance dermoscopy (sUVRD) for PRP and blue–white structureless areas ...
Handan Merve Erol Mart   +3 more
wiley   +1 more source

A cross sectional study of dermatoglyphics and dental caries in Bengalee children

open access: yesJournal of Indian Society of Pedodontics and Preventive Dentistry, 2013
Context: Dermatoglyphic is the permanent imprint found in hands. Variations of dermatoglyphic patterns among the individuals have been noted. Aims: To find out the dermatoglyphic pattern variations in dental caries between study group and the control ...
Asok bijoy sengupta   +5 more
doaj   +1 more source

Fingerprints Encode Risk for Bipolarity

open access: yesBipolar Disorders, Volume 28, Issue 3, May 2026.
ABSTRACT Background Fingerprint patterns are developed during pregnancy and share a common embryogenic origin with the central nervous system. Considering the observed relationship between prenatal abnormalities and higher risk for schizophrenia, we previously built fingerprint‐based algorithms achieving validation accuracies up to 70% in a large ...
Raymond Salvador   +25 more
wiley   +1 more source

Prenatal Diagnosis of Autosomal Recessive Primary Microcephaly Type 2 Caused by Compound Heterozygous WDR62 Variants in a Family With Two Recurrent Cases

open access: yesMolecular Genetics &Genomic Medicine, Volume 14, Issue 4, April 2026.
We report prenatal diagnosis of MCPH2 via trio‐WES, identifying novel compound heterozygous WDR62 variants. To our knowledge, prenatal MRI detection of lobar HPE and lissencephaly with the agyria–pachygyria complex has not been reported in fetuses with WDR62 variants. Consequently, these findings have advanced our understanding of prenatally detectable
Yan‐Fang Li   +3 more
wiley   +1 more source

Dermatoglyphics findings in intellectual disability children with down syndrome, autism spectrum disorder and attention-deficit hyperactivity disorder: A descriptive cross-sectional study

open access: yesAdvances in Human Biology, 2021
Introduction: Intellectual disability is a condition, in which mental development is incomplete or hindered, causing the individuals to encounter difficulties in everyday learning.
Astri Anindya Sariza   +4 more
doaj   +1 more source

Rapid Nasal Breathing as a Biometric Trigger: High‐Accuracy Electroencephalogram‐Based Authentication for Clinical Applications

open access: yesThe Clinical Respiratory Journal, Volume 20, Issue 1, January 2026.
Our study demonstrates rapid nasal breathing‐evoked EEG signals enable high‐accuracy (98.3%) biometric authentication via a hybrid ResNet‐Swin Transformer model. This noninvasive approach eliminates external stimuli, offering secure patient identification for critical respiratory care settings, such as ventilator access and continuous monitoring ...
Cai Chen   +8 more
wiley   +1 more source

Multiple Elements in Single Words [PDF]

open access: yes, 2019
What\u27s the shortest word from which the names of 2 chemical elements can be spelled ...
Francis, Darryl
core   +1 more source

Genotype–Phenotype Correlations, Mortality, and Clinical Insights in Keratitis–Ichthyosis–Deafness Syndrome: A Comprehensive Review and Case Report

open access: yesAmerican Journal of Medical Genetics Part A, Volume 197, Issue 11, November 2025.
ABSTRACT Keratosis–ichthyosis–deafness (KID) syndrome is a rare autosomal dominant ectodermal disease caused by mutations in the GJB2 gene, which encodes the gap junction protein Connexin 26 (Cx26) located on Chr. 13q12.11. This study presents the first mortality analysis associated with KID syndrome, focusing on a case report of a Latin American ...
Leslie Patrón‐Romero   +17 more
wiley   +1 more source

Types and frequency of fingerprint minutiae in individuals of Igbo and Yoruba ethnic groups of Nigeria

open access: yesRuhuna Journal of Science, 2019
The population distribution of fingerprint minutiae is necessary to improve efficiency of fingerprints in identifying individuals in a population-specific manner. The objective of the study was to determine the distribution of different types of minutiae
U. U. Akpan   +3 more
doaj   +1 more source

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