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American Journal of Medical Genetics. Part A
|
May 29, 2012
Germline mosacism in Shprintzen-Goldberg syndrome
Alan L Shanske, James T Goodrich, Leena Ala-Kokko, et al.
American Journal of Medical Genetics. Part A
|
July 31, 2008
Fine mapping of breakpoints in two unrelated patients with rare overlapping interstitial deletions of 9q with mild dysmorphic features
Anita S Kulharya, David B Flannery, Karen Norris, et al.
Fertility and Sterility
|
May 18, 2011
Use of single nucleotide polymorphism microarrays to distinguish between balanced and normal chromosomes in embryos from a translocation carrier
Nathan R Treff, Xin Tao, Wendy J Schillings, et al.
Genes
|
September 28, 2023
3' UTR Deletion of <i>FBXO28</i> in a Patient with Brain Abnormalities and Developmental Delay
Xin Bi, Maureen S Mulhern, Erica Spiegel, et al.
Biotechniques
|
February 15, 2020
A rapid and simple bead-bashing-based method for genomic DNA extraction from mammalian tissue
Shan Wei, Brynn Levy, Nataly Hoffman, et al.
Annals of Neurology
|
August 6, 2010
Glut1 deficiency: inheritance pattern determined by haploinsufficiency
Michael Rotstein, Kristin Engelstad, Hong Yang, et al.
Fertility and Sterility
|
July 9, 2004
Pregnancy after cryopreservation of donor oocytes and preimplantation genetic diagnosis of embryos in a patient with ovarian failure
Kathleen A Miller, Karen Elkind-Hirsch, Brynn Levy, et al.
Prenatal Diagnosis
|
November 24, 2020
Right or wrong? Looking through the retrospectoscope to analyse predictions made a decade ago in prenatal diagnosis and fetal surgery
Lyn S Chitty, Alessandro Ghidini, Jan Deprest, et al.
Journal of Assisted Reproduction and Genetics
|
October 25, 2017
At the dawn of personalized reproductive medicine: opportunities and challenges with incorporating multigene panel testing into fertility care
Piraye Yurttas Beim, David-Emlyn Parfitt, Lei Tan, et al.
Plos One
|
February 24, 2018
Validation of a SNP-based non-invasive prenatal test to detect the fetal 22q11.2 deletion in maternal plasma samples
Harini Ravi, Gabriel McNeill, Shruti Goel, et al.
Page
of 13
Search research articles
Search
Showing results (41-50 of 122) with videos related to
Sort By:
Page
of 13
American Journal of Medical Genetics. Part A
|
May 29, 2012
Germline mosacism in Shprintzen-Goldberg syndrome
Alan L Shanske, James T Goodrich, Leena Ala-Kokko, et al.
American Journal of Medical Genetics. Part A
|
July 31, 2008
Fine mapping of breakpoints in two unrelated patients with rare overlapping interstitial deletions of 9q with mild dysmorphic features
Anita S Kulharya, David B Flannery, Karen Norris, et al.
Fertility and Sterility
|
May 18, 2011
Use of single nucleotide polymorphism microarrays to distinguish between balanced and normal chromosomes in embryos from a translocation carrier
Nathan R Treff, Xin Tao, Wendy J Schillings, et al.
Genes
|
September 28, 2023
3' UTR Deletion of <i>FBXO28</i> in a Patient with Brain Abnormalities and Developmental Delay
Xin Bi, Maureen S Mulhern, Erica Spiegel, et al.
Biotechniques
|
February 15, 2020
A rapid and simple bead-bashing-based method for genomic DNA extraction from mammalian tissue
Shan Wei, Brynn Levy, Nataly Hoffman, et al.
Annals of Neurology
|
August 6, 2010
Glut1 deficiency: inheritance pattern determined by haploinsufficiency
Michael Rotstein, Kristin Engelstad, Hong Yang, et al.
Fertility and Sterility
|
July 9, 2004
Pregnancy after cryopreservation of donor oocytes and preimplantation genetic diagnosis of embryos in a patient with ovarian failure
Kathleen A Miller, Karen Elkind-Hirsch, Brynn Levy, et al.
Prenatal Diagnosis
|
November 24, 2020
Right or wrong? Looking through the retrospectoscope to analyse predictions made a decade ago in prenatal diagnosis and fetal surgery
Lyn S Chitty, Alessandro Ghidini, Jan Deprest, et al.
Journal of Assisted Reproduction and Genetics
|
October 25, 2017
At the dawn of personalized reproductive medicine: opportunities and challenges with incorporating multigene panel testing into fertility care
Piraye Yurttas Beim, David-Emlyn Parfitt, Lei Tan, et al.
Plos One
|
February 24, 2018
Validation of a SNP-based non-invasive prenatal test to detect the fetal 22q11.2 deletion in maternal plasma samples
Harini Ravi, Gabriel McNeill, Shruti Goel, et al.
Page
of 13