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Human Mutation
|
February 13, 2020
Critical assessment of secondary findings in genes linked to primary arrhythmia syndromes
Isabel Diebold, Ulrike Schön, Florentine Scharf, et al.
Familial Cancer
|
May 3, 2025
A series of reviews in familial cancer: genetic cancer risk in context variants of uncertain significance in MMR genes: which procedures should be followed?
Morghan C Lucas, Thomas Keßler, Florentine Scharf, et al.
Familial Cancer
|
May 15, 2022
Long-term chemoprevention in patients with adenomatous polyposis coli: an observational study
Teresa M Neuhann, Katharina Haub, Verena Steinke-Lange, et al.
European Journal of Human Genetics : EJHG
|
February 13, 2014
Biallelic MUTYH mutations can mimic Lynch syndrome
Monika Morak, Barbara Heidenreich, Gisela Keller, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society
|
April 23, 2015
Phosphatidylinositol 3-kinase (PI3K) signalling regulates insulin-like-growth factor binding protein-2 (IGFBP-2) production in human adipocytes
Franziska Wilhelm, Franziska Kässner, Gordian Schmid, et al.
Genetics in Medicine Open
|
March 3, 2025
Reclassification of VUS in <i>BRCA1</i> and <i>BRCA2</i> using the new <i>BRCA1</i>/<i>BRCA2</i> ENIGMA track set demonstrates the superiority of ClinGen ENIGMA Expert Panel specifications over the standard ACMG/AMP classification system
Anna Benet-Pagès, Andreas Laner, Luis R Nassar, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 7, 2004
Gene delivery systems--gene therapy vectors for cystic fibrosis
Daniel Klink, Dirk Schindelhauer, Andreas Laner, et al.
BMC Medical Genomics
|
April 1, 2021
HPO-driven virtual gene panel: a new efficient approach in molecular autopsy of sudden unexplained death
Ulrike Schön, Anna Holzer, Andreas Laner, et al.
Genes
|
January 26, 2024
Novel Homozygous FA2H Variant Causing the Full Spectrum of Fatty Acid Hydroxylase-Associated Neurodegeneration (SPG35)
Alexander German, Jelena Jukic, Andreas Laner, et al.
Familial Cancer
|
February 1, 2020
Prevalence of CNV-neutral structural genomic rearrangements in MLH1, MSH2, and PMS2 not detectable in routine NGS diagnostics
Monika Morak, Verena Steinke-Lange, Trisari Massdorf, et al.
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Search research articles
Search
Showing results (11-20 of 48) with videos related to
Sort By:
Page
of 5
Human Mutation
|
February 13, 2020
Critical assessment of secondary findings in genes linked to primary arrhythmia syndromes
Isabel Diebold, Ulrike Schön, Florentine Scharf, et al.
Familial Cancer
|
May 3, 2025
A series of reviews in familial cancer: genetic cancer risk in context variants of uncertain significance in MMR genes: which procedures should be followed?
Morghan C Lucas, Thomas Keßler, Florentine Scharf, et al.
Familial Cancer
|
May 15, 2022
Long-term chemoprevention in patients with adenomatous polyposis coli: an observational study
Teresa M Neuhann, Katharina Haub, Verena Steinke-Lange, et al.
European Journal of Human Genetics : EJHG
|
February 13, 2014
Biallelic MUTYH mutations can mimic Lynch syndrome
Monika Morak, Barbara Heidenreich, Gisela Keller, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society
|
April 23, 2015
Phosphatidylinositol 3-kinase (PI3K) signalling regulates insulin-like-growth factor binding protein-2 (IGFBP-2) production in human adipocytes
Franziska Wilhelm, Franziska Kässner, Gordian Schmid, et al.
Genetics in Medicine Open
|
March 3, 2025
Reclassification of VUS in <i>BRCA1</i> and <i>BRCA2</i> using the new <i>BRCA1</i>/<i>BRCA2</i> ENIGMA track set demonstrates the superiority of ClinGen ENIGMA Expert Panel specifications over the standard ACMG/AMP classification system
Anna Benet-Pagès, Andreas Laner, Luis R Nassar, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society
|
October 7, 2004
Gene delivery systems--gene therapy vectors for cystic fibrosis
Daniel Klink, Dirk Schindelhauer, Andreas Laner, et al.
BMC Medical Genomics
|
April 1, 2021
HPO-driven virtual gene panel: a new efficient approach in molecular autopsy of sudden unexplained death
Ulrike Schön, Anna Holzer, Andreas Laner, et al.
Genes
|
January 26, 2024
Novel Homozygous FA2H Variant Causing the Full Spectrum of Fatty Acid Hydroxylase-Associated Neurodegeneration (SPG35)
Alexander German, Jelena Jukic, Andreas Laner, et al.
Familial Cancer
|
February 1, 2020
Prevalence of CNV-neutral structural genomic rearrangements in MLH1, MSH2, and PMS2 not detectable in routine NGS diagnostics
Monika Morak, Verena Steinke-Lange, Trisari Massdorf, et al.
Page
of 5