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1. Back Cover, Volume 43, Issue 7. Issue 7 (8th June 2022)

2. Computational Investigation of Growth Hormone Receptor Trp169Arg Heterozygous Mutation in a Child With Short Stature. Issue 12 (9th June 2017)

4. IDR‐1018 induces cell proliferation, migration, and reparative gene expression in 2D culture and 3D human skin equivalents. (26th August 2019)

6. Pathogenic variants in the TRIP11 gene cause a skeletal dysplasia spectrum from odontochondrodysplasia to achondrogenesis 1A. Issue 4 (5th January 2020)

7. Phenotypic and mutational spectrum of ROR2‐related Robinow syndrome. Issue 7 (10th May 2022)

9. Short stature, unusual face, delta phalanx, and abnormal vertebrae and ribs in a girl born to half‐siblings. Issue 5 (31st March 2017)