C. Bommer

发表

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

K. Kalache, R. Chaoui, C. Tennstedt, 2002, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Karyotyping of human chondrocytes in scaffold-assisted cartilage tissue engineering.

M. Endres, C. Kaps, L. Morawietz, 2012, Acta biomaterialia.

Comparison of the Performance of QF-PCR with QPCR as A Rapid Molecular-Based Method for Sex Chromosome Aneuploidies Detection

H. Neitzel, R. Varon, V. Dutrannoy, 2014 .

De novo 9 Mb deletion of 6q23.2q24.1 disrupting the gene EYA4 in a patient with sensorineural hearing loss, cardiac malformation, and mental retardation.

S. Mundlos, E. Klopocki, L. Graul-Neumann, 2009, European journal of medical genetics.

BCR-ABL1+ Acute Myeloid Leukemia: Clonal Selection of a BCR-ABL1- Subclone as a Cause of Refractory Disease with Nilotinib Treatment

B. Dörken, M. Schwarz, T. Burmeister, 2014, Acta Haematologica.

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

B. Dörken, M. Schwarz, P. Daniel, 2010, Haematologica.

Prenatal diagnosis of classical phenylketonuria by linked restriction fragment length polymorphism analysis

O. Riess, C. Coutelle, A. Speer, 1986, Prenatal diagnosis.

Molecular characterization of a balanced chromosome translocation in psoriasis vulgaris

N. Tommerup, H. Ropers, V. Kalscheuer, 2005, Clinical genetics.

High-throughput sequencing of microdissected chromosomal regions

M. Grabherr, S. Mundlos, R. Reinhardt, 2010, European Journal of Human Genetics.

QF-PCR as a molecular-based method for autosomal aneuploidies detection

H. Neitzel, R. Varon, D. El-kaffash, 2013 .

Cells from Urine Sample

H. Körner, C. Bommer, Henrike Dia, 1999 .

Fetal Trisomy 10 Mosaicism: Ultrasound, Cytogenetic and Morphologic Findings in Early Pregnancy

H. Knoblauch, S. Tinschert, C. Tennstedt, 1999, Prenatal diagnosis.

Prenatal diagnosis of trisomy 1q21‐qter: Case report and review of literature

R. Chaoui, C. Bommer, A. Machlitt, 2005, American journal of medical genetics. Part A.

Bilaterally cleft lip, limb defects, and haematological manifestations: Roberts syndrome versus TAR syndrome.

S. Tinschert, H. Enders, M. Urban, 1998, American journal of medical genetics.

Ring chromosome 6 in three fetuses: case reports, literature review, and implications for prenatal diagnosis.

R. Wegner, R. Becker, C. Tennstedt, 2002, American journal of medical genetics.

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

T. Haaf, D. Galetzka, Y. Yue, 2007, European Journal of Human Genetics.

Prenatal diagnosis of an isochromosome 5p in a fetus with increased nuchal translucency thickness and pulmonary atresia with hypoplastic right heart at 14 weeks

R. Chaoui, C. Tennstedt, H. Körner, 2004, Prenatal diagnosis.

[Prenatal diagnosis of heart defects and associated chromosomal aberrations].

R. Chaoui, H. Körner, R. Bollmann, 1999, Ultraschall in der Medizin.

Cytogenetic studies in acute leukemia patients relapsing after allogeneic stem cell transplantation.

E. Thiel, A. Stroux, H. Neitzel, 2010, Cancer genetics and cytogenetics.

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

R. Chaoui, C. Tennstedt, H. Körner, 2002, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.