Related Experiment Videos
The Wagner-Stickler syndrome-a genetic study
Birth Defects Original Article Series
|January 1, 1979
Summary
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): a possible locus for Fryns syndrome.
American journal of medical genetics. Part A·2005
Craniofacial skeletal deviations following in utero exposure to the anticonvulsant phenytoin: monotherapy and polytherapy.
Orthodontics & craniofacial research·2003
Limb deficiencies in newborn infants.
Pediatrics·2001
Limb anomalies from evolutionary, developmental, and genetic perspectives.
Birth defects original article series·1996
Multisite neural tube closure in humans.
Birth defects original article series·1996
Low-Coverage Whole-Genome Sequencing Identifies Loci Associated with Birth Weight in East Friesian × Hu Crossbred Sheep.
Animals : an open access journal from MDPI·2026
Integrative MRI and Genomics Analyses Prioritize <i>PACSIN1</i> as a Candidate Gene for Cerebellar Ataxia in Border Collies.
Animals : an open access journal from MDPI·2026
Bayesian Population-Based Prevalence Estimation of <i>KCNV2</i>-Associated Retinopathy: A Comparative Analysis of Disease-Associated Variant Frequencies in Russian and Global Populations.
International journal of molecular sciences·2026