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1. HeterozygousCOL17A1variants are a frequent cause of amelogenesis imperfecta

5. Spectrum of pathogenic variants and founder effects in amelogenesis imperfecta associated with MMP20

6. Spectrum of pathogenic variants and multiple founder effects in amelogenesis imperfecta associated with MMP20

10. NovelDLX3variants in amelogenesis imperfecta with attenuated tricho‐dento‐osseous syndrome

16. Mutations in the pH-Sensing G-protein-Coupled Receptor GPR68 Cause Amelogenesis Imperfecta

18. Spectrum of PEX1 and PEX6 variants in Heimler syndrome

19. A homozygous STIM1 mutation impairs store-operated calcium entry and natural killer cell effector function without clinical immunodeficiency

20. A distinctive oral phenotype points to FAM 20A mutations not identified by S anger sequencing

21. Heimler Syndrome Is Caused by Hypomorphic Mutations in the Peroxisome-Biogenesis Genes PEX1 and PEX6

23. Variability of systemic and oro-dental phenotype in two families with non-lethal Raine syndrome with FAM20C mutations

29. Identification of Mutations in SLC24A4, Encoding a Potassium-Dependent Sodium/Calcium Exchanger, as a Cause of Amelogenesis Imperfecta

30. Mutations in C4orf26, Encoding a Peptide with In Vitro Hydroxyapatite Crystal Nucleation and Growth Activity, Cause Amelogenesis Imperfecta

33. Mutations in CNNM4 Cause Jalili Syndrome, Consisting of Autosomal-Recessive Cone-Rod Dystrophy and Amelogenesis Imperfecta

37. Identification of Microcephalin, a Protein Implicated in Determining the Size of the Human Brain

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