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European Journal of Human Genetics : EJHG|February 5, 2021
Origins of human genetics. A personal perspectiveEberhard PassargeAmerican Journal of Medical Genetics. Part A|March 27, 2016
James L. German, a pioneer in early human genetic research turned 90Eberhard PassargeDeutsche Medizinische Wochenschrift (1946)|December 5, 2022
[Thalidomide embryopathy 60 years]Eberhard PassargeEuropean Journal of Human Genetics : EJHG|February 11, 2016
Marfanoid-progeroid-lipodystrophy syndrome: a newly recognized fibrillinopathyEberhard Passarge, Peter N Robinson, Luitgard M Graul-NeumannPrenatal Diagnosis|February 8, 2003
Prenatally detected trisomy 4 and 6 mosaicism--cytogenetic results and clinical phenotypeDagmar Wieczorek, Eva C Prott, Wendy P Robinson, et al.European Journal of Medical Genetics|December 2, 2008
Three de novo losses and one insertion within a pericentric inversion of chromosome 6 in a patient with complete absence of expressive speech and reduced pain perceptionMartin Poot, Ruben van't Slot, Romina Leupert, et al.Human Genetics|February 4, 2016
Improved prediction of complex diseases by common genetic markers: state of the art and further perspectivesBent Müller, Arndt Wilcke, Anne-Laure Boulesteix, et al.American Journal of Medical Genetics. Part A|November 26, 2009
Two adults with Rubinstein-Taybi syndrome with mild mental retardation, glaucoma, normal growth and skull circumference, and camptodactyly of third fingersDagmar Wieczorek, Oliver Bartsch, Stanislav Lechno, et al.American Journal of Medical Genetics. Part A|October 28, 2010
Marfan syndrome with neonatal progeroid syndrome-like lipodystrophy associated with a novel frameshift mutation at the 3' terminus of the FBN1-geneLuitgard M Graul-Neumann, Tina Kienitz, Peter N Robinson, et al.Cell Reports|July 21, 2012
Constitutional chromothripsis rearrangements involve clustered double-stranded DNA breaks and nonhomologous repair mechanismsWigard P Kloosterman, Masoumeh Tavakoli-Yaraki, Markus J van Roosmalen, et al.Pageof 2