Katharina Schoner: search on Z-Library

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1

Klinefelter twins presenting with discordant aneuploidies, acardia, forked umbilical cord and with different gonadal sex despite monozygosity

Helga Rehder, Katharina Schoner, Britta Kluge, Frank Louwen, Eberhard Schwinger, Juergen Neesen

Journal:

Prenatal Diagnosis

Year:

2012

Language:

english

File:

PDF, 283 KB

english, 2012

2

Human parvovirus B19 infection causing discrepant prenatal findings and outcome in monochorionic diamniotic twins

Witteborn, Katharina, Schoner, Katharina, Enders, Martin, Gembruch, Ulrich, Arabin, Birgit

Journal:

Case Reports in Perinatal Medicine

Year:

2014

Language:

english

File:

PDF, 102 KB

english, 2014

3

Actin isoform expression patterns in adult extracardiac and cardiac rhabdomyomas indicate a different cell of origin

Westhoff, Christina C., Schoner, Katharina, Hartmann, Sylvia, Sesterhenn, Andreas M., Moll, Roland

Journal:

Virchows Archiv

Year:

2017

Language:

english

File:

PDF, 1.22 MB

english, 2017

4

Smith‐Lemli‐Opitz syndrome — Fetal phenotypes with special reference to the syndrome‐specific internal malformation pattern

Schoner, Katharina, Witsch‐Baumgartner, Martina, Behunova, Jana, Petrovic, Robert, Bald, Rainer, Kircher, Susanne G., Ramaswamy, Annette, Kluge, Britta, Meyer‐Wittkopf, Matthias, Schmitz, Ralf, Fritz,

Journal:

Birth Defects Research

Year:

2019

File:

PDF, 2.94 MB

2019

5

Recurrent Johanson-Blizzard Syndrome in a Triplet Pregnancy Complicated by Urethral Obstruction Sequence: A Clinical, Molecular, and Immunohistochemical Approach

Schoner, Katharina, Fritz, Barbara, Huelskamp, Georg, Louwen, Frank, Zenker, Martin, Moll, Roland, Rehder, Helga

Journal:

Pediatric and Developmental Pathology

Year:

2012

Language:

english

File:

PDF, 6.03 MB

english, 2012

6

Hydrocephalus, agenesis of the corpus callosum, and cleft lip/palate represent frequent associations in fetuses with Peters' plus syndrome and B3GALTL mutations. - Fetal PPS phenotypes, expanded by Dandy Walker cyst and encephalocele

Schoner, Katharina, Kohlhase, Juergen, Müller, Annette M., Schramm, Thomas, Plassmann, Margit, Schmitz, Ralf, Neesen, Juergen, Wieacker, Peter, Rehder, Helga

Journal:

Prenatal Diagnosis

Year:

2013

Language:

english

File:

PDF, 338 KB

english, 2013

7

Desbuquois dysplasia type I and fetal hydrops due to novel mutations in the CANT1 gene

Laccone, Franco, Schoner, Katharina, Krabichler, Birgit, Kluge, Britta, Schwerdtfeger, Robin, Schulze, Bernt, Zschocke, Johannes, Rehder, Helga

Journal:

European Journal of Human Genetics

Year:

2011

Language:

english

File:

PDF, 294 KB

english, 2011

8

Severe Facial Clefts in Acrofacial Dysostosis

Schoner, Katharina, Steinhard, Johannes, Figiel, Jens, Rehder, Helga

Journal:

Obstetrics & Gynecology

Year:

2008

Language:

english

File:

PDF, 482 KB

english, 2008

9

An in-vitro assessment of the shear bond strength of bulk-fill resin composites to permanent and deciduous teeth

Ilie, Nicoleta, Schöner, Christian, Bücher, Katharina, Hickel, Reinhard

Journal:

Journal of Dentistry

Year:

2014

Language:

english

File:

PDF, 258 KB

english, 2014

10

Piepkorn type of osteochondrodysplasia: Defining the severe end of FLNB -related skeletal disorders in three fetuses and a 106-year-old exhibit

Rehder, Helga, Laccone, Franco, Kircher, Susanne G., Schild, Ralf L., Rapp, Christiane, Bald, Rainer, Schulze, Bernt, Behunova, Jana, Neesen, Juergen, Schoner, Katharina

Journal:

American Journal of Medical Genetics Part A

Year:

2018

Language:

english

File:

PDF, 1.13 MB

english, 2018

11

Fetal Manifestation of the Fine-Lubinsky Syndrome

Schoner, Katharina, Bald, Rainer, Fritz, Barbara, Rehder, Helga

Journal:

Fetal Diagnosis and Therapy

Year:

2008

Language:

english

File:

PDF, 271 KB

english, 2008

12

Double-Outlet Left Ventricle in Association With Heterotaxy and Left Isomerism of the Atrial Appendages

Schoner, Katharina, Enzensberger, Christian, Vogel, Melanie, Degenhard, Jan, Rehder, Helga, Axt-Fliedner, Roland

Journal:

Journal of Ultrasound in Medicine

Year:

2012

Language:

english

File:

PDF, 751 KB

english, 2012

13

Mutations in TGDS associated with additional malformations of the middle fingers and halluces: Atypical Catel-Manzke syndrome in a fetus

Schoner, Katharina, Bald, Rainer, Horn, Denise, Rehder, Helga, Kornak, Uwe, Ehmke, Nadja

Journal:

American Journal of Medical Genetics Part A

Year:

2017

Language:

english

File:

PDF, 671 KB

english, 2017

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