Osteodysplastic primordial dwarfism: Report of a further patient with manifestations similar to those seen in patients with types I and III
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference5 articles.
1. Studies of microcephalic primordial dwarfism I: Approach to a delineation of the seckel syndrome
2. Studies of microcephalic primordial dwarfism II: The osteodysplastic type II of primordial dwarfism
3. Studies of microcephalic primordial dwarfism III: An intrauterine dwarf with platyspondyly and anomalies of pelvis and clavicles—osteodysplastic primordial dwarfism type III
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1. The expanding phenotype of RNU4ATAC pathogenic variants to Lowry Wood syndrome;American Journal of Medical Genetics Part A;2017-12-19
2. Microcephalic Osteodysplastic Primordial Dwarfism, Type II: a Clinical Review;Current Osteoporosis Reports;2017-04
3. Spontaneous malformations of the cerebellar vermis: Prevalence, inheritance, and relationship to lobule/fissure organization in the C57BL/6 lineage;Neuroscience;2015-12
4. A novel mutation inRNU4ATACin a patient with microcephalic osteodysplastic primordial dwarfism type I;American Journal of Medical Genetics Part A;2015-03-03
5. Further delineation of the clinical spectrum inRNU4ATACrelated microcephalic osteodysplastic primordial dwarfism type I;American Journal of Medical Genetics Part A;2013-06-21
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