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2. C Identification of the major genetic contributors to tetralogy of fallot. (May 2019)

3. Familial co-occurrence of congenital heart defects follows distinct patterns. (2nd July 2017)

4. 22q11.2 Deletion Syndrome is under-recognised in adult patients with tetralogy of Fallot and pulmonary atresia. Issue 8 (31st March 2010)

5. DNA methylation abundantly associates with fetal alcohol spectrum disorder and its subphenotypes. (May 2018)

6. No prominent role for complement C1-esterase inhibitor in Marfan syndrome mice. (30th November 2022)