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R J Galjaard

Showing results (1-10 of 14) with videos related to

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Prenatal Diagnosis|March 10, 2001
Follow-up investigations in uncultured amniotic fluid cells after uncertain cytogenetic resultsD Van Opstal, C van den Berg, R J Galjaard, et al.
Human Genetics|June 8, 2011
XCI in preimplantation mouse and human embryos: first there is remodelling…I M van den Berg, R J Galjaard, J S E Laven, et al.
Nature Genetics|January 1, 1997
De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndromeT Matsuura, J S Sutcliffe, P Fang, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 26, 2005
A virtual reality rendition of a fetal meningomyelocele at 32 weeks of gestationI A L Groenenberg, A H J Koning, R J Galjaard, et al.
American Journal of Medical Genetics|December 18, 2001
Lymphangiectasia with persistent Müllerian derivatives: confirmation of autosomal recessive Urioste syndromeM M van Haelst, J Hoogeboom, R J Galjaard, et al.
Human Reproduction (Oxford, England)|February 26, 2011
Defective deacetylation of histone 4 K12 in human oocytes is associated with advanced maternal age and chromosome misalignmentI M van den Berg, C Eleveld, M van der Hoeven, et al.
Prenatal Diagnosis|November 25, 1998
Abnormal karyotypes in semi-direct chorionic villus preparations of women with different cytogenetic risksF J Los, C van den Berg, D Van Opstal, et al.
European Journal of Human Genetics : EJHG|September 26, 2001
X-linked recessive inheritance of radial ray deficiencies in a family with four affected malesR J Galjaard, N Kostakoglu, J J Hoogeboom, et al.
American Journal of Medical Genetics|February 13, 2001
Differences in complexity of isolated brachydactyly type C cannot be attributed to locus heterogeneity aloneR J Galjaard, L I van der Ham, N A Posch, et al.
American Journal of Medical Genetics. Part A|June 14, 2006
Congenital diaphragmatic hernia associated with duplication of 11q23-qterM Klaassens, D A Scott, M van Dooren, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Prenatal Diagnosis|March 10, 2001
Follow-up investigations in uncultured amniotic fluid cells after uncertain cytogenetic resultsD Van Opstal, C van den Berg, R J Galjaard, et al.
Human Genetics|June 8, 2011
XCI in preimplantation mouse and human embryos: first there is remodelling…I M van den Berg, R J Galjaard, J S E Laven, et al.
Nature Genetics|January 1, 1997
De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndromeT Matsuura, J S Sutcliffe, P Fang, et al.
Ultrasound in Obstetrics & Gynecology : the Official Journal of the International Society of Ultrasound in Obstetrics and Gynecology|November 26, 2005
A virtual reality rendition of a fetal meningomyelocele at 32 weeks of gestationI A L Groenenberg, A H J Koning, R J Galjaard, et al.
American Journal of Medical Genetics|December 18, 2001
Lymphangiectasia with persistent Müllerian derivatives: confirmation of autosomal recessive Urioste syndromeM M van Haelst, J Hoogeboom, R J Galjaard, et al.
Human Reproduction (Oxford, England)|February 26, 2011
Defective deacetylation of histone 4 K12 in human oocytes is associated with advanced maternal age and chromosome misalignmentI M van den Berg, C Eleveld, M van der Hoeven, et al.
Prenatal Diagnosis|November 25, 1998
Abnormal karyotypes in semi-direct chorionic villus preparations of women with different cytogenetic risksF J Los, C van den Berg, D Van Opstal, et al.
European Journal of Human Genetics : EJHG|September 26, 2001
X-linked recessive inheritance of radial ray deficiencies in a family with four affected malesR J Galjaard, N Kostakoglu, J J Hoogeboom, et al.
American Journal of Medical Genetics|February 13, 2001
Differences in complexity of isolated brachydactyly type C cannot be attributed to locus heterogeneity aloneR J Galjaard, L I van der Ham, N A Posch, et al.
American Journal of Medical Genetics. Part A|June 14, 2006
Congenital diaphragmatic hernia associated with duplication of 11q23-qterM Klaassens, D A Scott, M van Dooren, et al.
Pageof 2