722 results on '"Offiah, A. C."'
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2. Test 8
3. Test 5
4. Test 9
5. Test 7
6. Test 4
7. Test 1
8. Test 2
9. Test 3
10. The incidence of fractures in children under two years of age: a systematic review
11. Disparities in paediatric radiology research publications from low- and lower middle-income countries: a time for change
12. “The accuracy of the EOS imaging system to assess hip abnormalities in adolescents and adults:” a systematic review and meta-analysis
13. Dyssegmental Dysplasia, HSPG2-Related
14. Catel-Manzke Syndrome, TGDS-Related
15. Apert Syndrome, FGFR2-Related
16. Otospondylomegaepiphyseal Dysplasia, Recessive and Dominant Types, COL11A2-Related
17. Melnick-Needles Syndrome (Osteodysplasty), FLNA-Related
18. Chondrodysplasia Punctata Tibia-Metacarpal Type
19. Stüve-Wiedemann Dysplasia, LFR-Related
20. Short Rib-Polydactyly Syndrome Type 2 (Majewski), NEK1-, DYNC2H1-, IFT81- and IFT154-Related
21. Thoracolaryngopelvic Dysplasia (Barnes)
22. Menkes Disease, ATP7A-Related
23. Meckel Syndrome, TMRM67-, CEP290-, RPGRIP1L-, CC2D2A MKS1-, TMEM216-, NPHP3-, TCTN2-, B9D1-, B9D2-, TMEM231-, KIF14-, TMEM107- and TXNDC15-Related
24. DK Phocomelia
25. Kniest Dysplasia, COL2A1-Related
26. Achondrogenesis Type 2/Hypochondrogenesis, COL2A1-Related
27. Dysplastic Cortical Hyperostosis, Kozlowski-Tsuruta Type
28. Dysplastic Cortical Hyperostosis, Al-Gazali Type, ADAMTSL2-Related
29. Brachydactyly Type C, GDF5-Related
30. Fibrochondrogenesis, COL11A1- and COL11A2-Related
31. Achondrogenesis (Type 1B), SLC26A2-Related
32. Schneckenbecken Dysplasia, SLC35D1-Related
33. Cousin Syndrome, TBX15-Related
34. Bruck Syndrome, FKBP10- and PLOD2-Related
35. Kaufman-McKusick Syndrome, MKKS-Related
36. Astley-Kendall Dysplasia
37. Uniparental Disomy, Paternal, for Chromosome 14 (UPD14; Kagami-Ogata Syndrome)
38. Diaphanospondylodysostosis, BMPER-Related
39. Rubinstein-Taybi Syndrome, CREBBP- and EP300-Related
40. Limb Reduction Syndrome (Al-Awadi Raas-Rothschild Limb-Pelvis Hypoplasia-Aplasia), WNT7A-Related
41. Blomstrand Dysplasia, PTHR1-Related
42. 3M Syndrome, CUL7-, OBSL1- and CCDC9-Related
43. Atelosteogenesis Type 3, FLNB-Related
44. Warfarin Embryopathy
45. OEIS Complex
46. Caffey Disease (Including Infantile and Attenuated Forms), COL1A1-Related
47. Dysosteosclerosis, SLC29A3-, TNFRSF11A- and CSF1R-Related
48. Yunis-Varon Dysplasia, FIG4- and VAC14-Related
49. Mesomelic Dysplasia, Kozlowski-Reardon Type
50. Saul-Wilson Syndrome, COG4-Related
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