Christiane Bommer

Absent or hypoplastic thymus on ultrasound: a marker for deletion 22q11.2 in fetal cardiac defects

Rabih Chaoui, Karim D. Kalache, K. S. Heling et al. · Ultrasound in Obstetrics and Gynecology · 2002 · 137 citations · Full text

De novo t(12;17)(p13.3;q21.3) translocation with a breakpoint near the 5′ end of the HOXB gene cluster in a patient with developmental delay and skeletal malformations

Ying Yue, R. Farcas, Gundula Thiel et al. · European Journal of Human Genetics · 2007 · 84 citations · Full text

Developmental Anomaly, Developmental Biology, Genetic Disorder +9

Impact of additional chromosomal aberrations and BCR-ABL kinase domain mutations on the response to nilotinib in Philadelphia chromosome-positive chronic myeloid leukemia

T. D. Kim, Seval Türkmen, Michaela Schwarz et al. · Haematologica · 2009 · 44 citations · Full text

Prenatal diagnosis of 22q11 microdeletion in an early second‐trimester fetus with conotruncal anomaly presenting with increased nuchal translucency and bilateral intracardiac echogenic foci

A. Machlitt, C. Tennstedt, H. Körner et al. · Ultrasound in Obstetrics and Gynecology · 2002 · 37 citations

High-throughput sequencing of microdissected chromosomal regions

Anja Weise, Bernd Timmermann, Manfred Grabherr et al. · European Journal of Human Genetics · 2009 · 27 citations · Full text

Sequence Assembly, Functional Genomics, Sequencing +7