Mosaic tetrasomy 20p associated with osteoporosis and recurrent fractures
Author:
Affiliation:
1. Department of Pediatrics; University of Hawaii John A. Burns School of Medicine; Honolulu Hawaii
2. Kapi'olani Medical Specialists; Honolulu Hawaii
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.37074/fullpdf
Reference16 articles.
1. De novo trisomy 20p characterized by array comparative genomic hybridization: Report of a novel case and review of the literature;Bartolini;Gene,2013
2. Bone morphogenetic proteins for spinal fusion;Carlisle;Spine J,2005
3. Isochromosome 20p associated with multiple congenital abnormalities;Fryer;Clin Dysmorphol,2005
4. 20p duplication as a result of parental translocation: Familial case report and a contribution to the clinical delineation of the syndrome;Grammatico;Clin Genet,1992
5. Bone Morphogenetic Protein-2 promotes osteoblast apoptosis through a Smad-independent, protein kinase C-dependent signaling pathway;Haÿ;J Biol Chem,2001
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