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.

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 (Concept Id: C0729582)

Floating-Harbor syndrome: MedlinePlus Genetics

Expanded spectrum of exon 33 and 34 mutations in SRCAP and follow-up in patients with Floating-Harbor syndrome, BMC Medical Genetics

48 New Genetic Variants Linked to Multiple Sclerosis

Floating Harbor Syndrome – Floating Harbor Syndrome Global Support

Myhre syndrome: MedlinePlus Genetics

Brain Sciences, Free Full-Text

Sotos Syndrome 2 disease: Malacards - Research Articles, Drugs, Genes, Clinical Trials

The first Finnish patient with the Floating‐Harbor syndrome: The follow‐up of eight years - Ala‐Mello - 2004 - American Journal of Medical Genetics Part A - Wiley Online Library

Floating-Harbor syndrome: Presentation of the first Romanian patient with a mutation and review of the literature

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

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

A diagram showing potential pathogenetic mechanisms underlying the

Frontiers Floating-Harbor Syndrome Treated With Recombinant Human Growth Hormone: A Case Report and Literature Review