H. Körner

发表

Spectrum of congenital heart defects and extracardiac malformations associated with chromosomal abnormalities: results of a seven year necropsy study

M. Dietel, R. Chaoui, C. Tennstedt, 1999, Heart.

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

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

Molecular characterization of a balanced chromosome translocation in psoriasis vulgaris

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

Clinical and molecular cytogenetic studies of a large de novo interstitial deletion 16q11.2-16q21 including the putative transcription factor geneSALL1

R. Chaoui, H. Knoblauch, S. Tinschert, 2000, Journal of medical genetics.

Phylloid Pigmentary Pattern with Mosaic Trisomy 13

D. Horn, H. Körner, Marisa Rommeck, 1997, Pediatric dermatology.

Pallister-Killian syndrome: normal karyotype in prenatal chorionic villi, in postnatal lymphocytes, and in slowly growing epidermal cells, but mosaic tetrasomy 12p in skin fibroblasts.

D. Horn, H. Körner, F. Majewski, 1995, Journal of medical genetics.

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.

12th Fetal Cell Workshop

P. Hufnagl, J. Foidart, M. Dietel, 2001, Fetal Diagnosis and Therapy.

Maternal serum alpha-fetoprotein screening for neural tube defects and other disorders using an ultramicro-ELISA

S. Tinschert, A. Horn, H. Körner, 1986, Human 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.

Correlation of prenatal ultrasound diagnosis and morphological findings of fetal autopsy.

M. Dietel, R. Chaoui, C. Tennstedt, 1998, Pathology, research and practice.

Fetal Autopsy: The Most Important Contribution of Pathology in a Center for Perinatal Medicine

P. Hufnagl, M. Dietel, R. Chaoui, 2001, Fetal Diagnosis and Therapy.

Fetal autopsy: a review of recent developments.

P. Hufnagl, M. Dietel, R. Chaoui, 2001, European journal of obstetrics, gynecology, and reproductive biology.

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.

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.

Translocation t(7p+; 13q-) associated with recurrent abortion

H. Körner, H. Agricola, H. Bayer, 1975, Human Genetics.