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Zeitschrift Fur Gastroenterologie|November 19, 2019
[Current recommendations for surveillance, risk reduction and therapy in Lynch syndrome patients]Robert Hüneburg, Stefan Aretz, Reinhard Büttner, et al.
The Journal of Investigative Dermatology|January 30, 2013
Androgenetic alopecia: identification of four genetic risk loci and evidence for the contribution of WNT signaling to its etiologyStefanie Heilmann, Amy K Kiefer, Nadine Fricker, et al.
Kidney International Reports|April 14, 2025
Trio Exome Sequencing in VACTERL AssociationJasmina Ćomić, Erik Tilch, Korbinian M Riedhammer, et al.
European Journal of Human Genetics : EJHG|October 27, 2011
Genome-wide pooling approach identifies SPATA5 as a new susceptibility locus for alopecia areataLina M Forstbauer, Felix F Brockschmidt, Valentina Moskvina, et al.
Nature Communications|January 23, 2015
Genome-wide meta-analysis in alopecia areata resolves HLA associations and reveals two new susceptibility lociRegina C Betz, Lynn Petukhova, Stephan Ripke, et al.
The Journal of Clinical Investigation|June 11, 2026
Biallelic inactivating variants in the chromatin remodeler DMAP1 cause a syndromic neurodevelopmental disorderQin Wang, Andrew K Sobering, Christian Tirrito, et al.
European Journal of Cancer (Oxford, England : 1990)|March 20, 2021
Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants: a Prospective Lynch Syndrome Database reportToni T Seppälä, Mev Dominguez-Valentin, Emma J Crosbie, et al.
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