Osteogenesis imperfecta and the family: A qualitative analysis of the experiences of family and caregivers.
Gianna M. Colombo(Baylor College of Medicine), Eric A. Storch(University of Florida), Amelia Mercado(Michael E. DeBakey VA Medical Center), Sophie C. Schneider(Baylor College of Medicine), Marie‐Eve Robinson(University of Ottawa), Julia Morales(Baylor College of Medicine), Kara Ayers(GC Systems (United States)), Brendan Lee(Baylor College of Medicine), Kristin M. Kostick(Baylor College of Medicine), Chaya N. Murali(Baylor College of Medicine), V. Reid Sutton(Baylor College of Medicine), Andrew D. Wiese(Baylor College of Medicine), Saniah Ishtiaq Kazimi(Baylor College of Medicine), W. Conor Rork(Columbia College), Members Of the BBDC, Michelle L. Fynan, Whitney S. Shepherd(Baylor College of Medicine), Dianne Nguyen(Baylor College of Medicine), Hannah E. Cho(Baylor College of Medicine)
Cited by 0
Related Papers
Resolution of Disease Phenotypes Resulting from Multilocus Genomic Variation
|New England Journal of Medicine|2016|774
IRF2BPL Is Associated with Neurological Phenotypes
|The American Journal of Human Genetics|2018|115
MicroRNA miR-23a cluster promotes osteocyte differentiation by regulating TGF-β signalling in osteoblasts
|Nature Communications|2017|96
Phenylbutyrate therapy for maple syrup urine disease
|Human Molecular Genetics|2010|94
Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay
|The American Journal of Human Genetics|2018|91