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You searched for: Author/Creator Warner, Neil

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1. 25 MUTATIONS IN STXBP3 CONTRIBUTE TO VERY EARLY ONSET OF IBD, IMMUNODEFICIENCY AND HEARING LOSS. (18th January 2018)

2. Application of Whole Exome Sequencing in Congenital Secretory Diarrhea Diagnosis. Issue 6 (June 2019)

3. Chromosomal Numerical Aberrations and Rare Copy Number Variation in Patients with Inflammatory Bowel Disease. (30th July 2022)

4. Human ALPI deficiency causes inflammatory bowel disease and highlights a key mechanism of gut homeostasis. Issue 4 (22nd March 2018)

5. Platelet VPS16B is dependent on VPS33B expression, as determined in two siblings with arthrogryposis, renal dysfunction, and cholestasis syndrome. (12th April 2022)

6. UTILIZATION OF WHOLE EXOME SEQUENCING DATA TO IDENTIFY CLINICALLY RELEVANT PHARMACOGENOMIC VARIANTS IN INFLAMMATORY BOWEL DISEASE. (21st January 2021)

7. Utilization of Whole Exome Sequencing Data to Identify Clinically Relevant Pharmacogenomic Variants in Pediatric Inflammatory Bowel Disease. Issue 12 (1st December 2020)

8. Variants in STXBP3 are Associated with Very Early Onset Inflammatory Bowel Disease, Bilateral Sensorineural Hearing Loss and Immune Dysregulation. (23rd April 2021)