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Saethre-Chotzen syndrome
(phenotype)
Summary
General Info
Genetic Markers
Most Correlated Genes
Most Correlated SNPs
TWIST1
FGFR2
No SNPs found
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Pathway Enrichment
Most Correlated Biogroups
cranial skeletal system development
embryonic cranial skeleton morphogenesis
regulation of ossification
ossification
mesenchymal cell differentiation
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Curated Studies
Most Correlated Studies
OMIM - Saethre-Chotzen syndrome
Mouse Phenotypes - Craniosynostosis
OMIM - Congenital disorder
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Literature
Most Relevant Literature
Prenatal diagnosis of a 7p15-p21 deletion encompassing the TWIST1 gene involved in Saethre-Chotzen s…
Interrelationship of cranial suture fusion, basicranial development, and resynostosis following sutu…
Saethre-Chotzen syndrome: a case report.
The frequency of palatal anomalies in Saethre-Chotzen syndrome.
Saethre-Chotzen Syndrome, Pro136His TWIST Mutation, Hearing Loss, and External and Middle Ear Struct…
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Clinical Trials
Most Relevant Clinical Trials
GROWing Up With Rare GENEtic Syndromes
Craniosynostosis :Surgical Treatment Modalities and Outcome
Genetic Studies of Strabismus, Congenital Cranial Dysinnervation Disorders (CCDDs), and Their Associ…
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