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

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

A schematic of the SRCAP gene and comparison of SRCAP-conserved ATPase

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Myhre syndrome: MedlinePlus Genetics

Myhre syndrome: MedlinePlus Genetics

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

The promise of whole-exome sequencing in medical genetics

Coffin-Siris Syndrome 4 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

Clinical features of Floating Harbor Syndrome in our patient. Small

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

Angelman syndrome: MedlinePlus Genetics

Floating-Harbor syndrome: MedlinePlus Genetics