Lista de obras -

Aberrant right subclavian artery (ARSA)--a new sonographic marker for chromosomal aberrations in the second trimester--preliminary observations

artículo científico publicado en 2014

Clinical significance of the prenatal double bubble sign - single institution experience

artículo científico publicado en 2015

Complex malformations involving the fetal body wall - definition and classification issues.

artículo científico publicado en 2017

First trimester pregnancy loss: Clinical implications of genetic testing.

artículo científico publicado en 2016

First-trimester spontaneous pregnancy loss - molecular analysis using multiplex ligation-dependent probe amplification

artículo científico publicado en 2016

Foeto-maternal haemorrhage: An unexpected challenge

artículo científico publicado en 2017

In-house genetic counseling increases the detection of abnormal karyotypes-a 26-year experience in prenatal diagnosis in a single tertiary referral hospital in Poland

scientific article published on 19 May 2020

Increased nuchal translucency in chromosomally normal fetuses and pregnancy outcomes – a retrospective study ⬇️

artículo científico publicado el 1 de marzo de 2013

Maternal blood intrauterine transfusions in the therapy of red-cell alloimmunization performed in three difficult cases

artículo científico publicado en 2014

Maternal complications in molecularly confirmed diandric and digynic triploid pregnancies: single institution experience and literature review

artículo científico publicado en 2020

Multiplex ligation-dependent probe amplification (MLPA)--new possibilities of prenatal diagnosis.

artículo científico publicado en 2013

Prenatal diagnosis and clinical significance of cephalocele-A single institution experience and literature review

artículo científico publicado en 2020

Prenatal diagnosis of Duchenne and Becker muscular dystrophies: Underestimated problem of the secondary prevention of monogenetic disorders

artículo científico publicado en 2017

Prenatal diagnosis of congenital myopathies and muscular dystrophies.

artículo científico publicado en 2016

Prenatal diagnosis of craniosynostosis (compound Saethre-Chotzen syndrome phenotype) caused by a de novo complex chromosomal rearrangement (1; 4; 7) with a microdeletion of 7p21.3-7p15.3, including TWIST1 gene--a case report

article

Skin-covered bladder exstrophy diagnosed antenatally.

artículo científico publicado en 2013

Targeted prenatal diagnosis of Pallister-Killian syndrome.

artículo científico publicado en 2017

The location of the fetal ears: A hint for prenatal diagnosis of agnathia-otocephaly complex

scientific article published on 12 February 2019

Triploidy - variability of sonographic phenotypes.

artículo científico publicado en 2017

Usefulness of methylation-specific multiplex ligation-dependent probe amplification for identification of parental origin of triploidy

scientific article published on 01 June 2020

[Effectiveness of multiplex ligation dependent probe amplification (MLPA) in prenatal diagnosis of common aneuploidies]

scientific article published on 01 August 2013

[Metformin in pregnancy]

scientific article published on 01 July 2014

[Non-invasive prenatal diagnosis of the most common aneuploidies with cell-free fetal DNA in maternal serum--preliminary results]

artículo científico publicado en 2014

[Noninvasive prenatal diagnosis of trisomy 21, 18 and 13 using cell-free fetal DNA].

artículo científico publicado en 2013

Lista de obras de

Aberrant right subclavian artery (ARSA)--a new sonographic marker for chromosomal aberrations in the second trimester--preliminary observations

Clinical significance of the prenatal double bubble sign - single institution experience

Complex malformations involving the fetal body wall - definition and classification issues.

First trimester pregnancy loss: Clinical implications of genetic testing.

First-trimester spontaneous pregnancy loss - molecular analysis using multiplex ligation-dependent probe amplification

Foeto-maternal haemorrhage: An unexpected challenge

In-house genetic counseling increases the detection of abnormal karyotypes-a 26-year experience in prenatal diagnosis in a single tertiary referral hospital in Poland

Increased nuchal translucency in chromosomally normal fetuses and pregnancy outcomes – a retrospective study ⬇️

Maternal blood intrauterine transfusions in the therapy of red-cell alloimmunization performed in three difficult cases

Maternal complications in molecularly confirmed diandric and digynic triploid pregnancies: single institution experience and literature review

Multiplex ligation-dependent probe amplification (MLPA)--new possibilities of prenatal diagnosis.

Prenatal diagnosis and clinical significance of cephalocele-A single institution experience and literature review

Prenatal diagnosis of Duchenne and Becker muscular dystrophies: Underestimated problem of the secondary prevention of monogenetic disorders

Prenatal diagnosis of congenital myopathies and muscular dystrophies.

Prenatal diagnosis of craniosynostosis (compound Saethre-Chotzen syndrome phenotype) caused by a de novo complex chromosomal rearrangement (1; 4; 7) with a microdeletion of 7p21.3-7p15.3, including TWIST1 gene--a case report

Skin-covered bladder exstrophy diagnosed antenatally.

Targeted prenatal diagnosis of Pallister-Killian syndrome.

The location of the fetal ears: A hint for prenatal diagnosis of agnathia-otocephaly complex

Triploidy - variability of sonographic phenotypes.

Usefulness of methylation-specific multiplex ligation-dependent probe amplification for identification of parental origin of triploidy

[Effectiveness of multiplex ligation dependent probe amplification (MLPA) in prenatal diagnosis of common aneuploidies]

[Metformin in pregnancy]

[Non-invasive prenatal diagnosis of the most common aneuploidies with cell-free fetal DNA in maternal serum--preliminary results]

[Noninvasive prenatal diagnosis of trisomy 21, 18 and 13 using cell-free fetal DNA].