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.

Floating Harbor Syndrome – Floating Harbor Syndrome Global Support

Overview of Floating Harbor Syndrome

Floating harbour syndrome with medial entropion: a rare association and brief review

Floating Harbor Syndrome (FHS) - DoveMed

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

Floating-Harbor syndrome: MedlinePlus Genetics

Therapeutic advantages of combined gene/cell therapy strategies in a murine model of GM2 gangliosidosis: Molecular Therapy - Methods & Clinical Development

Otopalatodigital Syndrome, Type I disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

Chiari I malformation as part of the Floating-Harbor syndrome? - ScienceDirect

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Rare-disease genetics in the era of next-generation sequencing: discovery to translation