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Matthias Begemann

Showing results (1-10 of 97) with videos related to

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Clinical Epigenetics|February 5, 2021
Unusual deletion of the maternal 11p15 allele in Beckwith-Wiedemann syndrome with an impact on both imprinting domainsThomas Eggermann, Matthias Begemann, Lutz Pfeiffer
Orphanet Journal of Rare Diseases|June 25, 2010
Silver-Russell syndrome: genetic basis and molecular genetic testingThomas Eggermann, Matthias Begemann, Gerhard Binder, et al.
Best Practice & Research. Clinical Endocrinology & Metabolism|March 15, 2011
Silver-Russell syndromeGerhard Binder, Matthias Begemann, Thomas Eggermann, et al.
European Journal of Medical Genetics|May 18, 2019
Contribution of GRB10 to the prenatal phenotype in Silver-Russell syndrome? Lessons from 7p12 copy number variationsThomas Eggermann, Matthias Begemann, Ingo Kurth, et al.
European Journal of Human Genetics : EJHG|November 22, 2020
Biallelic PADI6 variants cause multilocus imprinting disturbances and miscarriages in the same familyThomas Eggermann, Gundula Kadgien, Matthias Begemann, et al.
Genetic Testing and Molecular Biomarkers|May 27, 2011
Testing of buccal swab DNA does not increase the detection rate for imprinting control region 1 hypomethylation in Silver-Russell syndromeSabrina Spengler, Matthias Begemann, Gerhard Binder, et al.
European Journal of Medical Genetics|October 3, 2020
Molecular characterization of temple syndrome families with 14q32 epimutationsJohanna Brück, Matthias Begemann, Daniela Dey, et al.
American Journal of Medical Genetics. Part A|January 17, 2012
Segmental maternal uniparental disomy 7q associated with DLK1/GTL2 (14q32) hypomethylationMatthias Begemann, Sabrina Spengler, Ulrike Kordass, et al.
Molecular and Cellular Probes|January 6, 2019
Next generation sequencing and imprinting disorders: Current applications and future perspectives: Lessons from Silver-Russell syndromeLea Neuheuser, Robert Meyer, Matthias Begemann, et al.
Epigenomics|December 1, 2011
Disturbed methylation at multiple imprinted loci: an increasing observation in imprinting disordersThomas Eggermann, Isabelle Leisten, Gerhard Binder, et al.
Pageof 10

Showing results (1-10 of 97) with videos related to

Sort By:
Pageof 10
Clinical Epigenetics|February 5, 2021
Unusual deletion of the maternal 11p15 allele in Beckwith-Wiedemann syndrome with an impact on both imprinting domainsThomas Eggermann, Matthias Begemann, Lutz Pfeiffer
Orphanet Journal of Rare Diseases|June 25, 2010
Silver-Russell syndrome: genetic basis and molecular genetic testingThomas Eggermann, Matthias Begemann, Gerhard Binder, et al.
Best Practice & Research. Clinical Endocrinology & Metabolism|March 15, 2011
Silver-Russell syndromeGerhard Binder, Matthias Begemann, Thomas Eggermann, et al.
European Journal of Medical Genetics|May 18, 2019
Contribution of GRB10 to the prenatal phenotype in Silver-Russell syndrome? Lessons from 7p12 copy number variationsThomas Eggermann, Matthias Begemann, Ingo Kurth, et al.
European Journal of Human Genetics : EJHG|November 22, 2020
Biallelic PADI6 variants cause multilocus imprinting disturbances and miscarriages in the same familyThomas Eggermann, Gundula Kadgien, Matthias Begemann, et al.
Genetic Testing and Molecular Biomarkers|May 27, 2011
Testing of buccal swab DNA does not increase the detection rate for imprinting control region 1 hypomethylation in Silver-Russell syndromeSabrina Spengler, Matthias Begemann, Gerhard Binder, et al.
European Journal of Medical Genetics|October 3, 2020
Molecular characterization of temple syndrome families with 14q32 epimutationsJohanna Brück, Matthias Begemann, Daniela Dey, et al.
American Journal of Medical Genetics. Part A|January 17, 2012
Segmental maternal uniparental disomy 7q associated with DLK1/GTL2 (14q32) hypomethylationMatthias Begemann, Sabrina Spengler, Ulrike Kordass, et al.
Molecular and Cellular Probes|January 6, 2019
Next generation sequencing and imprinting disorders: Current applications and future perspectives: Lessons from Silver-Russell syndromeLea Neuheuser, Robert Meyer, Matthias Begemann, et al.
Epigenomics|December 1, 2011
Disturbed methylation at multiple imprinted loci: an increasing observation in imprinting disordersThomas Eggermann, Isabelle Leisten, Gerhard Binder, et al.
Pageof 10