131 results on '"Offiah, A. C."'
Search Results
2. Catel-Manzke Syndrome, TGDS-Related
3. Apert Syndrome, FGFR2-Related
4. Otospondylomegaepiphyseal Dysplasia, Recessive and Dominant Types, COL11A2-Related
5. Melnick-Needles Syndrome (Osteodysplasty), FLNA-Related
6. Chondrodysplasia Punctata Tibia-Metacarpal Type
7. Stüve-Wiedemann Dysplasia, LFR-Related
8. Short Rib-Polydactyly Syndrome Type 2 (Majewski), NEK1-, DYNC2H1-, IFT81- and IFT154-Related
9. Thoracolaryngopelvic Dysplasia (Barnes)
10. Menkes Disease, ATP7A-Related
11. Meckel Syndrome, TMRM67-, CEP290-, RPGRIP1L-, CC2D2A MKS1-, TMEM216-, NPHP3-, TCTN2-, B9D1-, B9D2-, TMEM231-, KIF14-, TMEM107- and TXNDC15-Related
12. DK Phocomelia
13. Kniest Dysplasia, COL2A1-Related
14. Achondrogenesis Type 2/Hypochondrogenesis, COL2A1-Related
15. Dysplastic Cortical Hyperostosis, Kozlowski-Tsuruta Type
16. Dysplastic Cortical Hyperostosis, Al-Gazali Type, ADAMTSL2-Related
17. Brachydactyly Type C, GDF5-Related
18. Fibrochondrogenesis, COL11A1- and COL11A2-Related
19. Achondrogenesis (Type 1B), SLC26A2-Related
20. Schneckenbecken Dysplasia, SLC35D1-Related
21. Cousin Syndrome, TBX15-Related
22. Bruck Syndrome, FKBP10- and PLOD2-Related
23. Kaufman-McKusick Syndrome, MKKS-Related
24. Astley-Kendall Dysplasia
25. Uniparental Disomy, Paternal, for Chromosome 14 (UPD14; Kagami-Ogata Syndrome)
26. Diaphanospondylodysostosis, BMPER-Related
27. Rubinstein-Taybi Syndrome, CREBBP- and EP300-Related
28. Limb Reduction Syndrome (Al-Awadi Raas-Rothschild Limb-Pelvis Hypoplasia-Aplasia), WNT7A-Related
29. Blomstrand Dysplasia, PTHR1-Related
30. 3M Syndrome, CUL7-, OBSL1- and CCDC9-Related
31. Atelosteogenesis Type 3, FLNB-Related
32. Warfarin Embryopathy
33. OEIS Complex
34. Caffey Disease (Including Infantile and Attenuated Forms), COL1A1-Related
35. Dysosteosclerosis, SLC29A3-, TNFRSF11A- and CSF1R-Related
36. Yunis-Varon Dysplasia, FIG4- and VAC14-Related
37. Mesomelic Dysplasia, Kozlowski-Reardon Type
38. Saul-Wilson Syndrome, COG4-Related
39. Femoral Facial Syndrome
40. Stickler Syndrome, COL2A1-Related
41. Achondroplasia, FGFR3-Related
42. Cranioectodermal Dysplasia (Levin-Sensenbrenner), IFTI22-, WDR35-, WDR19-, IFT40- and IFT43-Related
43. Short Rib-Polydactyly Syndrome Type 1 and 3, IFT80-, DYNC2H1-, WDR34-, WDR60- and DYNC2L11-Related
44. Metaphyseal Dysplasia, Jansen Type, PTHR1-Related
45. Short Rib-Polydactyly Syndrome Type 4 (Beemer), IFT80-Related
46. Mirror-Image Polydactyly of Hands and Feet (Laurin-Sandrow), SHH-Related
47. Schinzel-Giedion Syndrome, SETBP1-Related
48. Brachydactyly Temtamy Type, CHSY1-Related
49. Maternal Systemic Lupus Erythematosus
50. Robinow Syndrome, Recessive and Dominant Types, ROR2-, NXN-, WNT5A-, DVL1-, DVL3- and FZD2-Related
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