Related Experiment Videos
[Dermatoglyphics in mongolism. A diagnostic, prognostic and genetic counseling aid]
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
ASPP2 deficiency causes features of 1q41q42 microdeletion syndrome.
Cell death and differentiation·2016
Provisionally unique autosomal recessive syndrome due to significant consanguinity.
American journal of medical genetics·2001
Syndrome of microcephaly, mental retardation, and tracheoesophageal fistula associated with features of Rett syndrome.
Journal of child neurology·2000
Ring 2 chromosome: ten-year follow-up report.
American journal of medical genetics·1999
Radiological and orthopedic abnormalities in Satoyoshi syndrome.
Pediatric radiology·1997
Epidemiology of Obstructive Sleep Apnea in Chile: A Systematic Review and Meta-Analysis.
Revista medica de Chile·2026
Rescue of a Discarded Liver Graft Through Viability Assessment Using Normothermic Ex Vivo Machine Perfusion.
Revista medica de Chile·2026
Integrative Analysis of Nucleotide Metabolism-Related Genes Reveals a Diagnostic Signature and In Silico Functional Disruption in Hypertrophic Scarring.
Journal of burn care & research : official publication of the American Burn Association·2026