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Martin Krapp

Showing results (11-20 of 19) with videos related to

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The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|March 18, 2011
Prenatal detection and postnatal management of double outlet right ventricle (DORV) in 21 singleton pregnanciesDavid Rafael Hartge, Linda Niemeyer, Roland Axt-Fliedner, et al.
European Journal of Medical Genetics|July 13, 2007
Reduced penetrance in a family with X-linked dominant chondrodysplasia punctataYorck Hellenbroich, Karl-Heinz Grzeschik, Martin Krapp, et al.
Archives of Gynecology and Obstetrics|June 22, 2017
Fetal cephaloceles: prenatal diagnosis and course of pregnancy in 65 consecutive casesJan Weichert, Friederike Hoellen, Martin Krapp, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|June 24, 2005
The syndrome of left isomerism: sonographic findings and outcome in prenatally diagnosed casesChristoph Berg, Annegret Geipel, Daniel Kamil, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|January 30, 2020
Prenatal Diagnosis and Outcome of Congenital Corrected Transposition of the Great Arteries - A Multicenter Report of 69 CasesCarina Nina Vorisek, Christian Enzensberger, Steven Willomeit, et al.
Prenatal Diagnosis|June 17, 2017
Absent pulmonary valve syndrome - diagnosis, associations, and outcome in 71 prenatally diagnosed casesRoland Axt-Fliedner, Andrii Kurkevych, Maciej Slodki, et al.
Prenatal Diagnosis|February 2, 2023
Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variantsIvonne Bedei, Tascha Gehrke, Karl-Philipp Gloning, et al.
Prenatal Diagnosis|January 5, 2023
Turner syndrome-omphalocele association: Incidence, karyotype, phenotype and fetal outcomeIvonne Bedei, Karl-Philipp Gloning, Luc Joyeux, et al.
Journal of Clinical Medicine|August 12, 2022
Is Fetal Hydrops in Turner Syndrome a Risk Factor for the Development of Maternal Mirror Syndrome?Ivonne Alexandra Bedei, Alexander Graf, Karl-Philipp Gloning, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|March 18, 2011
Prenatal detection and postnatal management of double outlet right ventricle (DORV) in 21 singleton pregnanciesDavid Rafael Hartge, Linda Niemeyer, Roland Axt-Fliedner, et al.
European Journal of Medical Genetics|July 13, 2007
Reduced penetrance in a family with X-linked dominant chondrodysplasia punctataYorck Hellenbroich, Karl-Heinz Grzeschik, Martin Krapp, et al.
Archives of Gynecology and Obstetrics|June 22, 2017
Fetal cephaloceles: prenatal diagnosis and course of pregnancy in 65 consecutive casesJan Weichert, Friederike Hoellen, Martin Krapp, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|June 24, 2005
The syndrome of left isomerism: sonographic findings and outcome in prenatally diagnosed casesChristoph Berg, Annegret Geipel, Daniel Kamil, et al.
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|January 30, 2020
Prenatal Diagnosis and Outcome of Congenital Corrected Transposition of the Great Arteries - A Multicenter Report of 69 CasesCarina Nina Vorisek, Christian Enzensberger, Steven Willomeit, et al.
Prenatal Diagnosis|June 17, 2017
Absent pulmonary valve syndrome - diagnosis, associations, and outcome in 71 prenatally diagnosed casesRoland Axt-Fliedner, Andrii Kurkevych, Maciej Slodki, et al.
Prenatal Diagnosis|February 2, 2023
Multicenter clinical experience with non-invasive cell-free DNA screening for monosomy X and related X-chromosome variantsIvonne Bedei, Tascha Gehrke, Karl-Philipp Gloning, et al.
Prenatal Diagnosis|January 5, 2023
Turner syndrome-omphalocele association: Incidence, karyotype, phenotype and fetal outcomeIvonne Bedei, Karl-Philipp Gloning, Luc Joyeux, et al.
Journal of Clinical Medicine|August 12, 2022
Is Fetal Hydrops in Turner Syndrome a Risk Factor for the Development of Maternal Mirror Syndrome?Ivonne Alexandra Bedei, Alexander Graf, Karl-Philipp Gloning, et al.
Pageof 2