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1. 27 CLINICAL AND GENOMIC CORRELATES OF NEUTROPHIL GRANULOCYTE-MACROPHAGE COLONY STIMULATING FACTOR SIGNALING IN PEDIATRIC CROHN DISEASE. (18th January 2018)

2. Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects. Issue 1 (1st January 2018)

4. Disruption of RAB40AL function leads to Martin–Probst syndrome, a rare X-linked multisystem neurodevelopmental human disorder. Issue 5 (11th May 2012)

5. Enhanced Contribution of HLA in Pediatric Onset Ulcerative Colitis. Issue 4 (19th March 2018)

6. Enhanced Contribution of HLA in Pediatric Onset Ulcerative Colitis. Issue 4 (19th March 2018)

7. Genetic and Transcriptomic Variation Linked to Neutrophil Granulocyte–Macrophage Colony-Stimulating Factor Signaling in Pediatric Crohn's Disease. Issue 3 (13th August 2018)

8. Genetic and Transcriptomic Variation Linked to Neutrophil Granulocyte–Macrophage Colony-Stimulating Factor Signaling in Pediatric Crohn's Disease. Issue 3 (21st February 2019)

9. Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects. Issue 10 (1st October 2015)

10. Site- and Taxa-Specific Disease-Associated Oral Microbial Structures Distinguish Inflammatory Bowel Diseases. Issue 12 (14th May 2021)