Floating-Harbor syndrome: MedlinePlus Genetics
Por um escritor misterioso
Descrição
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: MedlinePlus Genetics
Angelman 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
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 (Concept Id: C0729582)
The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP, Orphanet Journal of Rare Diseases
Novel genotypes and phenotypes among Chinese patients with Floating-Harbor syndrome, Orphanet Journal of Rare Diseases
A diagram showing potential pathogenetic mechanisms underlying the
Floating-Harbor syndrome: MedlinePlus Genetics
The phenotype of Floating-Harbor syndrome: clinical characterization of 52 individuals with mutations in exon 34 of SRCAP, Orphanet Journal of Rare Diseases
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