Floating-Harbor syndrome: MedlinePlus Genetics

Floating-Harbor syndrome is a disorder involving short stature, slowing of the mineralization of the bones (delayed bone age), delayed speech development, and characteristic facial features. Explore symptoms, inheritance, genetics of this condition.

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Floating-Harbor syndrome: MedlinePlus Genetics

Search for a gene responsible for Floating‐Harbor syndrome on chromosome 12q15q21.1 - Lopez - 2012 - American Journal of Medical Genetics Part A - Wiley Online Library

Schematic representation of convergence of chromatinopathies.

Floating-Harbor syndrome: MedlinePlus Genetics

Mutations in SRCAP, Encoding SNF2-Related CREBBP Activator Protein, Cause Floating-Harbor Syndrome - ScienceDirect

Frontiers Molecular Genetics and Pathogenesis of the Floating Harbor Syndrome: Case Report of Long-Term Growth Hormone Treatment and a Literature Review

PDF) A rare cause of short stature: the floating harbor syndrome

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Floating Harbor Syndrome by roxan ghossein

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The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP, Orphanet Journal of Rare Diseases