B. Pertl

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Cell-Free DNA Testing for Fetal Chromosomal Anomalies in clinical practice: Austrian-German-Swiss Recommendations for non-invasive prenatal tests (NIPT)

P. Klaritsch, E. Merz, M. Schmid, 2015, Ultraschall in der Medizin.

Fetal nucleated red blood cells in peripheral blood of pregnant women: detection and determination of location on a slide using laser‐scanning cytometry

P. Kroisel, R. Wintersteiger, G. Dohr, 2003, Prenatal diagnosis.

First trimester prenatal diagnosis: fetal cells in the maternal circulation.

D. Bianchi, B. Pertl, Diana W. Bianchi, 1999, Seminars in perinatology.

Separation of sperm and vaginal cells based on ploidy, MHC class I-, CD45-, and cytokeratin expression for enhancement of DNA typing after sexual assault.

D. Strunk, M. Klintschar, B. Pertl, 1999, Cytometry.

Separation of sperm and vaginal cells with flow cytometry for DNA typing after sexual assault.

M. Klintschar, B. Pertl, W. Schoell, 1999, Obstetrics and gynecology.

Cystic periventricular leukomalacia in preterm infants: an analysis of obstetric risk factors.

U. Lang, M. Bauer, B. Resch, 2009, Early human development.

The Fetal Posterior Fossa on Prenatal Ultrasound Imaging: Normal Longitudinal Development and Posterior Fossa Anomalies

S. Verheyen, B. Pertl, Sophie Eder, 2019, Ultraschall in der Medizin - European Journal of Ultrasound.

Female fetal cells in maternal blood: use of DNA polymorphisms to prove origin

D. Bianchi, S. Sohda, A. Sekizawa, 2000, Human Genetics.

Detection of male and female fetal DNA in maternal plasma by multiplex fluorescent polymerase chain reaction amplification of short tandem repeats

D. Bianchi, A. Sekizawa, B. Pertl, 2000, Human Genetics.

Fetal microchimerism is not involved in the pathogenesis of lichen sclerosus of the vulva

W. Weger, U. Lang, B. Pertl, 2006, Prenatal diagnosis.

Rapid molecular method for prenatal detection of Down's syndrome

M. Adinolfi, J. Sherlock, B. Pertl, 1994, The Lancet.

Maternal interleukin-6 (−174) C/C polymorphism is associated with chorioamnionitis and cystic periventricular leucomalacia of the preterm infant

C. Mannhalter, J. Haas, B. Resch, 2010, Journal of Perinatology.

Maternal urine for prenatal diagnosis—an analysis of cell‐free fetal DNA in maternal urine and plasma in the third trimester

U. Lang, M. Bauer, B. Pertl, 2007, Prenatal diagnosis.

Genetic variations in fetal and maternal tumor necrosis factor-α and interleukin 10: is there an association with preterm birth or periventricular leucomalacia?

A. Griesbacher, U. Lang, B. Resch, 2012, Journal of Perinatology.

Prenatal detection of chromosome aneuploidy by quantitative fluorescence PCR.

E. Petek, B. Pertl, K. Mann, 2008, Methods in molecular biology.

Rapid detection of aneuploidies by microsatellite and the quantitative fluorescent polymerase chain reaction

M. Adinolfi, J. Sherlock, B. Pertl, 1997, Prenatal diagnosis.

Fetal DNA in Maternal Plasma: Emerging Clinical Applications

D. Bianchi, B. Pertl, 2001, Obstetrics and gynecology.

Detection of maternal deoxyribonucleic acid in umbilical cord plasma by using fluorescent polymerase chain reaction amplification of short tandem repeat sequences.

D. Bianchi, M. Bauer, B. Pertl, 2002, American journal of obstetrics and gynecology.

Detection and relocation of cord blood nucleated red blood cells by laser scanning cytometry.

B. Tiran, E. Petek, P. Kroisel, 2002, Cytometry.

Rapid detection of selected aneuploidies by quantitative fluorescent PCR.

M. Adinolfi, J. Sherlock, B. Pertl, 1995, BioEssays : news and reviews in molecular, cellular and developmental biology.

Prenatal Screening for Aneuploidies by Quantitative Fluorescent Polymerase Chain Reaction

V. Cirigliano, M. Adinolfi, J. Sherlock, 2001, Public Health Genomics.

Rapid prenatal diagnosis of aneuploidy by quantitative fluorescent PCR on fetal samples from mothers at high risk for chromosome disorders.

M. Adinolfi, P. Kroisel, B. Pertl, 1999, Molecular human reproduction.

Rapid detection of chromosome aneuploidies by quantitative fluorescence PCR: first application on 247 chorionic villus samples

B. Brambati, L. Tului, M. Adinolfi, 1999, Journal of medical genetics.

Rapid detection of trisomies 21 and 18 and sexing by quantitative fluorescent multiplex PCR

M. Adinolfi, J. Sherlock, P. Kroisel, 1996, Human Genetics.

Rapid and simple prenatal diagnosis of common chromosome disorders: advantages and disadvantages of the molecular methods FISH and QF-PCR.

S. Dhanjal, M. Hultén, B. Pertl, 2003, Reproduction.

Quantitative fluorescence polymerase chain reaction for the rapid prenatal detection of common aneuploidies and fetal sex.

M. Adinolfi, J. Sherlock, P. Kroisel, 1997, American journal of obstetrics and gynecology.

Diagnosis of trisomy 21 in fetal nucleated erythrocytes from maternal blood by use of short tandem repeat sequences.

D. Bianchi, S. Sohda, B. Pertl, 2001, Clinical chemistry.

SRY-specific cell free fetal DNA in maternal plasma in twin pregnancies throughout gestation.

A. Griesbacher, K. Orendi, U. Lang, 2011, Placenta.

Role of microchimerism in the pathogenesis of oral lichen planus

H. Kerl, L. Cerroni, W. Weger, 2006, Experimental dermatology.

Prenatal detection of chromosome aneuploidy by quantitative-fluorescence PCR.

Kathy Mann, E. Petek, B. Pertl, 2011, Methods in molecular biology.

Preterm twin gestation and cystic periventricular leucomalacia

B. Resch, B. Pertl, U. Maurer, 2004, Archives of Disease in Childhood - Fetal and Neonatal Edition.

[Effect of ultrasound examination on fetal version of breech presentation].

B. Pertl, F. Kainer, C. Fast, 1994, Geburtshilfe und Frauenheilkunde.

A prospective analysis of cell‐free fetal DNA concentration in maternal plasma as an indicator for adverse pregnancy outcome

G. Hutterer, D. Bianchi, M. Bauer, 2006, Prenatal diagnosis.

On targeting cell-free DNA in urine: a protocol for optimized DNA analysis.

M. Bauer, B. Pertl, 2009, Clinical chemistry.

[Value of ultrasound in early detection of endometrial carcinoma].

B. Pertl, A. Giuliani, M. Lahousen, 1996, Gynakologisch-geburtshilfliche Rundschau.

Diagnosis of chromosomal aneuploidies using quantitative fluorescent PCR.

M. Adinolfi, B. Pertl, 1998, Methods in molecular medicine.

Characterisation of a 19-year-old "long-term survivor" with Edwards syndrome.

M. Bauer, E. Petek, P. Kroisel, 2003, Genetic counseling.

RhD genotyping by quantitative fluorescent polymerase chain reaction: a new approach

B. Brambati, L. Tului, M. Adinolfi, 2000, BJOG : an international journal of obstetrics and gynaecology.

Preterm twin gestation and cystic periventricular leucomalacia

B. Resch, B. Pertl, U. Maurer, 2004, Archives of Disease in Childhood - Fetal and Neonatal Edition.

Targeted enrichment sequencing in two midterm pregnancies with severe abnormalities on ultrasound

P. Klaritsch, B. Tiran, P. Kroisel, 2017, The Lancet.

interleukin 10: is there an association with preterm birth or periventricular leucomalacia?

A. Griesbacher, U. Lang, B. Resch, 2011 .

Cell-Free DNA Testing for Fetal Chromosomal Anomalies in clinical practice : Austrian-German-Swiss Recommendations for non-invasive prenatal tests ( NIPT ) Drei

P. Klaritsch, E. Merz, M. Schmid, 2015 .

Quantitative florescent PCR for the rapid prenatal detection of common aneuploides and fetal sex

M. Adinolfi, J. Sherlock, P. Kroisel, 1997 .