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10. Biallelic Mutation of ARHGEF18, Involved in the Determination of Epithelial Apicobasal Polarity, Causes Adult-Onset Retinal Degeneration

11. Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa

14. Late-Onset Autosomal Dominant Macular Degeneration Caused by Deletion of the CRX Gene

16. Prevalence and architecture of de novo mutations in developmental disorders

17. Author Correction: CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

18. Loss-of-Function Mutations in the CFH Gene Affecting Alternatively Encoded Factor H-like 1 Protein Cause Dominant Early-Onset Macular Drusen

19. Psychosocial impact of undergoing prostate cancer screening for men with BRCA1 or BRCA2 mutations

20. CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language

21. Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

22. Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia

23. Task-Specific Training in Huntington Disease: A Randomized Controlled Feasibility Trial

24. Histone Lysine Methylases and Demethylases in the Landscape of Human Developmental Disorders

26. Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study

27. Biallelic Mutations in the Autophagy Regulator DRAM2 Cause Retinal Dystrophy with Early Macular Involvement

29. Mutations in REEP6 Cause Autosomal-Recessive Retinitis Pigmentosa

31. The ancient art of banking coals.

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