Search

Search Constraints

You searched for: Author/Creator Burfeind, Peter

Search Results

1. A 3p interstitial deletion in two monozygotic twin brothers and an 18‐year‐old man: Further characterization and review. Issue 10 (15th August 2013)

2. Intellectual disability associated with craniofacial dysmorphism, cleft palate, and congenital heart defect due to a de novo MEIS2 mutation: A clinical longitudinal study. Issue 4 (11th January 2021)

3. Loss-of-function variants in DNM1 cause a specific form of developmental and epileptic encephalopathy only in biallelic state. Issue 6 (25th June 2021)

4. Phenotypic spectrum of BLM‐ and RMI1‐related Bloom syndrome. Issue 5 (11th March 2022)

5. Simultaneous inhibition of IGF1R and EGFR enhances the efficacy of standard treatment for colorectal cancer by the impairment of DNA repair and the induction of cell death. (28th October 2017)