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Neck

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[Clinical characteristics and genetic analysis of a child with Coffin-Siris syndrome type 8 due to an intronic variant of SMARCC2 gene].
Neck
Clinical utility of image-guided core needle biopsy for axillary lymph node lesions suspected of lymphoproliferative disorders
Neck
Expanding the Phenotypic Spectrum Associated With Loss-of-Function SMARCA4 Variants to Eye Developmental Anomalies.
Neck
A de novo SOX11 mutation causing hypogonadotropic hypogonadism: a case report and literature review.
Neck
A novel variant in ARID2 causes Coffin-Siris syndrome 6 with liver cirrhosis.
Neck
Prenatal Sonographic Features and Genotype–Phenotype Correlations in Coffin–Siris Syndrome: A Systematic Case Analysis of 32 Fetuses
Neck
A Nonlinear Biomechanical Model for Prognostic Analysis of Clavicle Fractures
Neck
ANKRD17 Gene Heterozygous Variant Leads to Chopra-Amiel-Gordon Syndrome: A Case Study and Literature Review
Neck
Expanding the Coffin-Siris syndrome spectrum: genetic, dysmorphic, and endocrine findings in eight cases.
Neck
Chromatin remodelling subunit SMARCB1 is implicated in dendrite development and complex brain functions.
Neck

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