Floating-Harbor syndrome: MedlinePlus Genetics
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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 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
Clinical features of Floating Harbor Syndrome in our patient. Small
Search for a gene responsible for Floating‐Harbor syndrome on chromosome 12q15q21.1 - Lopez - 2012 - American Journal of Medical Genetics Part A - Wiley Online Library
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
Facial features of individuals with proximal and distal truncating
IJMS, Free Full-Text
What causes deep-set eyes? Symptoms of a rare disease
A diagram showing potential pathogenetic mechanisms underlying the
Mutations in SRCAP, Encoding SNF2-Related CREBBP Activator Protein, Cause Floating-Harbor Syndrome - ScienceDirect
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