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Birgit Sikkema-Raddatz

Showing results (1-10 of 60) with videos related to

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Human Mutation|March 8, 2012
Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consentWybo Dondorp, Birgit Sikkema-Raddatz, Christine de Die-Smulders, et al.
Expert Review of Molecular Diagnostics|November 5, 2014
Targeted next-generation sequencing panels for monogenetic disorders in clinical diagnostics: the opportunities and challengesTom J de Koning, Jan D H Jongbloed, Birgit Sikkema-Raddatz, et al.
Human Mutation|April 11, 2012
Genome-wide arrays in routine diagnostics of hematological malignanciesAnnet Simons, Birgit Sikkema-Raddatz, Nicole de Leeuw, et al.
European Journal of Medical Genetics|March 31, 2009
The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: report on two patients and review of the literatureAnnick Raas-Rothschild, Trijnie Dijkhuizen, Birgit Sikkema-Raddatz, et al.
Biology of Reproduction|July 19, 2013
Temporal and developmental-stage variation in the occurrence of mitotic errors in tripronuclear human preimplantation embryosEleni Mantikou, Jannie van Echten-Arends, Birgit Sikkema-Raddatz, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
Madelung deformity in a girl with a novel and de novo mutation in the GNAS genePatrick Rump, Jan D H Jongbloed, Birgit Sikkema-Raddatz, et al.
Prenatal Diagnosis|July 6, 2006
Quality aspects of prenatal cytogenetic diagnosis: determining the effect of various factors involved in handling amniotic fluid and chorionic villus material for cytogenetic diagnosisBirgit Sikkema-Raddatz, Ron Suijkerbuijk, Katelijne Bouman, et al.
Prenatal Diagnosis|July 6, 2006
An absolute procedure to test the growth potential of medium and the influence of decreased oxygen tension in primary amniotic fluid cell culturesBirgit Sikkema-Raddatz, Ron Suijkerbuijk, Jakob van der Vlag, et al.
European Journal of Medical Genetics|March 10, 2009
A unique 970kb microdeletion in 9q33.3, including the NR5A1 gene in a 46,XY femaleAnneke van Silfhout, Annemieke M Boot, Trijnie Dijkhuizen, et al.
Human Reproduction Update|May 3, 2011
Chromosomal mosaicism in human preimplantation embryos: a systematic reviewJannie van Echten-Arends, Sebastiaan Mastenbroek, Birgit Sikkema-Raddatz, et al.
Pageof 6

Showing results (1-10 of 60) with videos related to

Sort By:
Pageof 6
Human Mutation|March 8, 2012
Arrays in postnatal and prenatal diagnosis: An exploration of the ethics of consentWybo Dondorp, Birgit Sikkema-Raddatz, Christine de Die-Smulders, et al.
Expert Review of Molecular Diagnostics|November 5, 2014
Targeted next-generation sequencing panels for monogenetic disorders in clinical diagnostics: the opportunities and challengesTom J de Koning, Jan D H Jongbloed, Birgit Sikkema-Raddatz, et al.
Human Mutation|April 11, 2012
Genome-wide arrays in routine diagnostics of hematological malignanciesAnnet Simons, Birgit Sikkema-Raddatz, Nicole de Leeuw, et al.
European Journal of Medical Genetics|March 31, 2009
The 8q22.1 microdeletion syndrome or Nablus mask-like facial syndrome: report on two patients and review of the literatureAnnick Raas-Rothschild, Trijnie Dijkhuizen, Birgit Sikkema-Raddatz, et al.
Biology of Reproduction|July 19, 2013
Temporal and developmental-stage variation in the occurrence of mitotic errors in tripronuclear human preimplantation embryosEleni Mantikou, Jannie van Echten-Arends, Birgit Sikkema-Raddatz, et al.
American Journal of Medical Genetics. Part A|September 13, 2011
Madelung deformity in a girl with a novel and de novo mutation in the GNAS genePatrick Rump, Jan D H Jongbloed, Birgit Sikkema-Raddatz, et al.
Prenatal Diagnosis|July 6, 2006
Quality aspects of prenatal cytogenetic diagnosis: determining the effect of various factors involved in handling amniotic fluid and chorionic villus material for cytogenetic diagnosisBirgit Sikkema-Raddatz, Ron Suijkerbuijk, Katelijne Bouman, et al.
Prenatal Diagnosis|July 6, 2006
An absolute procedure to test the growth potential of medium and the influence of decreased oxygen tension in primary amniotic fluid cell culturesBirgit Sikkema-Raddatz, Ron Suijkerbuijk, Jakob van der Vlag, et al.
European Journal of Medical Genetics|March 10, 2009
A unique 970kb microdeletion in 9q33.3, including the NR5A1 gene in a 46,XY femaleAnneke van Silfhout, Annemieke M Boot, Trijnie Dijkhuizen, et al.
Human Reproduction Update|May 3, 2011
Chromosomal mosaicism in human preimplantation embryos: a systematic reviewJannie van Echten-Arends, Sebastiaan Mastenbroek, Birgit Sikkema-Raddatz, et al.
Pageof 6