Pages that link to "Q40946787"

The following pages link to What's in a face? (Q40946787):

Displaying 25 items.

• A genome-wide association study identifies five loci influencing facial morphology in Europeans (Q21563366) (← links)
• Minor physical anomalies in autism: a meta-analysis (Q22251104) (← links)
• Human and murine PTX1/Ptx1 gene maps to the region for Treacher Collins syndrome (Q28251879) (← links)
• Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome (Q28298470) (← links)
• AP-2-null cells disrupt morphogenesis of the eye, face, and limbs in chimeric mice (Q28586197) (← links)
• Copy number variation in intron 1 of SOX5 causes the Pea-comb phenotype in chickens (Q33466726) (← links)
• Submicroscopic deletions at 16p13.3 in Rubinstein-Taybi syndrome: frequency and clinical manifestations in a North American population (Q33678528) (← links)
• 22q11 deletion syndrome: a genetic subtype of schizophrenia (Q33745688) (← links)
• Discriminating power of localized three-dimensional facial morphology (Q34137531) (← links)
• Genetics of craniofacial development and malformation (Q34271559) (← links)
• Patterns of dysmorphic features in schizophrenia (Q35124133) (← links)
• Genetic determination of human facial morphology: links between cleft-lips and normal variation (Q35406172) (← links)
• Classification and visualization based on derived image features: application to genetic syndromes (Q35431730) (← links)
• Atypical face shape and genomic structural variants in epilepsy (Q36315335) (← links)
• Encephalocraniocutaneous lipomatosis syndrome in a child: association with multiple high flow cerebral arteriovenous fistulae. Case report and review (Q37769298) (← links)
• The functional matrix hypothesis revisited. 4. The epigenetic antithesis and the resolving synthesis (Q41621799) (← links)
• Craniofacial abnormalities induced by the ectopic expression of homeobox genes (Q41685028) (← links)
• Neurodevelopmental and neuroprogressive processes in schizophrenia. Antithetical or complementary, over a lifetime trajectory of disease? (Q41743488) (← links)
• Facial measurements in clinical genetics: How important are the instruments we use? (Q47758335) (← links)
• Signalling interactions during facial development (Q48394973) (← links)
• Late diagnosis in severe and mild intellectual disability in adulthood. (Q51937600) (← links)
• Computer-based recognition of dysmorphic faces (Q52011715) (← links)
• Distinctive facial features in idiopathic Moyamoya disease in Caucasians: a first systematic analysis. (Q55411851) (← links)
• Six NSCL/P Loci Show Associations With Normal-Range Craniofacial Variation (Q58556165) (← links)
• Quantification of Facial Traits. (Q64885930) (← links)