When the face says it all: dysmorphology in identifying syndromic causes of epilepsy.

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Exploring the Underlying Genetics of Craniofacial Morphology through Various Sources of Knowledge.

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When the face says it all: dysmorphology in identifying syndromic causes of epilepsy.

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2016 nî lūn-bûn

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When the face says it all: dysmorphology in identifying syndromic causes of epilepsy.

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When the face says it all: dysmorphology in identifying syndromic causes of epilepsy.

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When the face says it all: dysmorphology in identifying syndromic causes of epilepsy.

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When the face says it all: dysmorphology in identifying syndromic causes of epilepsy.

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Hirschsprung disease, microcephaly, mental retardation, and characteristic facial features: delineation of a new syndrome and identification of a locus at chromosome 2q22-q23

Clinical and molecular delineation of the 17q21.31 microdeletion syndrome

Cutaneous features in 17q21.31 deletion syndrome: a differential diagnosis for cardio-facio-cutaneous syndrome

Loss-of-function mutations in euchromatin histone methyl transferase 1 (EHMT1) cause the 9q34 subtelomeric deletion syndrome

Nicolaides-Baraitser syndrome: Delineation of the phenotype

Epilepsy in Mowat-Wilson syndrome: delineation of the electroclinical phenotype

Mutations in TCF4, encoding a class I basic helix-loop-helix transcription factor, are responsible for Pitt-Hopkins syndrome, a severe epileptic encephalopathy associated with autonomic dysfunction

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Genotype-phenotype associations in Sotos syndrome: an analysis of 266 individuals with NSD1 aberrations.

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10.1136/PRACTNEUROL-2015-001247

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When the face says it all: dysmorphology in identifying syndromic causes of epilepsy.

about

P2860

P2860

When the face says it all: dysmorphology in identifying syndromic causes of epilepsy.

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