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Rainer Bald

Showing results (11-20 of 17) with videos related to

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Transfusion|February 22, 2011
A new platelet alloantigen, Swi(a) , located on glycoprotein Ia identified in a family with fetal and neonatal alloimmune thrombocytopeniaHartmut Kroll, Korinna Feldmann, Claudia Zwingel, et al.
The Journal of Infectious Diseases|January 26, 2012
Serological and virological analysis of maternal and fetal blood samples in prenatal human parvovirus b19 infectionJohannes Weiffenbach, Rainer Bald, Karl-Philipp Gloning, et al.
American Journal of Medical Genetics. Part A|May 26, 2018
Piepkorn type of osteochondrodysplasia: Defining the severe end of FLNB-related skeletal disorders in three fetuses and a 106-year-old exhibitHelga Rehder, Franco Laccone, Susanne G Kircher, et al.
Archives of Gynecology and Obstetrics|August 2, 2022
Intrauterine transfusion in 103 fetuses with severe anemia caused by parvovirus infection. A multicenter retrospective studyPhilipp Kosian, Astrid Hellmund, Annegret Geipel, et al.
European Journal of Human Genetics : EJHG|January 20, 2012
Deletions in PITX1 cause a spectrum of lower-limb malformations including mirror-image polydactylyEva Klopocki, Christian Kähler, Nicola Foulds, et al.
Birth Defects Research|December 17, 2019
Smith-Lemli-Opitz syndrome - Fetal phenotypes with special reference to the syndrome-specific internal malformation patternKatharina Schoner, Martina Witsch-Baumgartner, Jana Behunova, et al.
Vox Sanguinis|March 1, 2003
Prenatal management of alloimmune thrombocytopenia of the fetusC P Engelfriet, H W Reesink, Hartmut Kroll, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Transfusion|February 22, 2011
A new platelet alloantigen, Swi(a) , located on glycoprotein Ia identified in a family with fetal and neonatal alloimmune thrombocytopeniaHartmut Kroll, Korinna Feldmann, Claudia Zwingel, et al.
The Journal of Infectious Diseases|January 26, 2012
Serological and virological analysis of maternal and fetal blood samples in prenatal human parvovirus b19 infectionJohannes Weiffenbach, Rainer Bald, Karl-Philipp Gloning, et al.
American Journal of Medical Genetics. Part A|May 26, 2018
Piepkorn type of osteochondrodysplasia: Defining the severe end of FLNB-related skeletal disorders in three fetuses and a 106-year-old exhibitHelga Rehder, Franco Laccone, Susanne G Kircher, et al.
Archives of Gynecology and Obstetrics|August 2, 2022
Intrauterine transfusion in 103 fetuses with severe anemia caused by parvovirus infection. A multicenter retrospective studyPhilipp Kosian, Astrid Hellmund, Annegret Geipel, et al.
European Journal of Human Genetics : EJHG|January 20, 2012
Deletions in PITX1 cause a spectrum of lower-limb malformations including mirror-image polydactylyEva Klopocki, Christian Kähler, Nicola Foulds, et al.
Birth Defects Research|December 17, 2019
Smith-Lemli-Opitz syndrome - Fetal phenotypes with special reference to the syndrome-specific internal malformation patternKatharina Schoner, Martina Witsch-Baumgartner, Jana Behunova, et al.
Vox Sanguinis|March 1, 2003
Prenatal management of alloimmune thrombocytopenia of the fetusC P Engelfriet, H W Reesink, Hartmut Kroll, et al.
Pageof 2