Christian Wentzel

Clinical variability of the 22q11.2 duplication syndrome

Christian Wentzel, Maria Fernström, Ylva Öhrner et al. · European Journal of Medical Genetics · 2008 · 222 citations · Full text

Genetic Disorder, Genetics, Duplication Syndrome +3

Induction of embryonic dysmorphogenesis by high glucose concentration, disturbed inositol metabolism, and inhibited protein kinase C activity

Parri Wentzel, Christian Wentzel, Mattias Gäreskog et al. · Teratology · 2001 · 73 citations

Mutations in <i>HECW2</i> are associated with intellectual disability and epilepsy

Jonatan Halvardson, Jin Zhao, Ammar Zaghlool et al. · Journal of Medical Genetics · 2016 · 68 citations · Full text

Genomic and clinical characteristics of six patients with partially overlapping interstitial deletions at 10p12p11

Christian Wentzel, Evica Rajcan‐Separovic, Claudia Ruivenkamp et al. · European Journal of Human Genetics · 2011 · 60 citations · Full text

Interstitial Deletions, Medicine, Genetics +8

A maternal de novo non-reciprocal translocation results in a 6q13-q16 deletion in one offspring and a 6q13-q16 duplication in another

Christian Wentzel, Göran Annerén, Ann‐Charlotte Thuresson · European Journal of Medical Genetics · 2014 · 38 citations