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.

Disorders of Chromosome 16 - DoveMed

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

Floating-Harbor syndrome - Medical Definition and Pronunciation

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

Genetic and pharmacologic proteasome augmentation ameliorates Alzheimer's-like pathology in mouse and fly APP overexpression models

The promise of whole-exome sequencing in medical genetics

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

Two patients with EP300 mutations and facial dysmorphism different from the classic Rubinstein–Taybi syndrome - Bartsch - 2010 - American Journal of Medical Genetics Part A - Wiley Online Library

Angelman syndrome: MedlinePlus Genetics

Vestibular CCK signaling drives motion sickness–like behavior in mice