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facial dysmorphism
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Genetic Markers
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ANIC
CHD3
PHIP
WDR26
OTUD6B
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Pathway Enrichment
Most Correlated Biogroups
odontogenesis
embryonic organ morphogenesis
limb morphogenesis
regulation of animal organ morphogenesis
JAEGER_METASTASIS_DN
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Curated Studies
Most Correlated Studies
Dental pulp stem cells from non-syndromic cleft lip palate (NSCL/P) patients
Calvaria with Axin2 knockout and heterozygous Runx2
Facial mesenchyme of E11.5 embryos from a mouse model for of cleft lip and palate (CLP) susceptibili
Orbicularis oris mesenchymal stem cells from patients with cleft lip with or without cleft palate
Mouse Phenotypes - Amelogenesis imperfecta
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Literature
Most Relevant Literature
Recessive truncating NALCN mutation in infantile neuroaxonal dystrophy with facial dysmorphism.
An interstitial 20q11.21 microdeletion causing mild intellectual disability and facial dysmorphisms.
Association of seizure, facial dysmorphism, congenital umbilical hernia and undescended testes.
Microdeletion 11q13.1.q13.2 in a patient presenting with developmental delay, facial dysmorphism, an…
Clinical and cytogenetic study of a case with familial chromosomal translocation presenting with fac…
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Clinical Trials
Most Relevant Clinical Trials
Marfan Syndrome (MFS) and Facial Dysmorphism: Non-invasive 3D Assessment
Effectiveness of Levetiracetam in the Treatment of Body Dysmorphic Disorder
Attentional Bias in Body Dysmorphic Disorder
Natural History in CCFDN and IBM Syndromes
Consequences of DNA Repair and Telomere Defects on the Function of the Immune System: Application to…
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