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American Journal of Medical Genetics. Part A|October 24, 2014
Twenty-one years to the right diagnosis - clinical overlap of Simpson-Golabi-Behmel and Beckwith-Wiedemann syndromeC Knopp, S Rudnik-Schöneborn, K Zerres, et al.Annales De Genetique|June 9, 2004
Unbalanced translocation 8;Y (45,X,dic(Y;8)(q11.23;p23.1)): case report and review of terminal 8p deletionsK Bosse, T Eggermann, K Van der Ven, et al.Alcohol and Alcoholism (Oxford, Oxfordshire)|April 4, 2015
Alcohol Consumption in Healthy OPRM1 G Allele Carriers and Its Association with Impulsive BehaviorP Pfeifer, M Sariyar, T Eggermann, et al.Annales De Genetique|August 6, 1999
Biparental expression of IGFBP1 and IGFBP3 renders their involvement in the etiology of Silver-Russell syndrome unlikelyK Eggermann, H A Wollmann, G Binder, et al.Human Heredity|June 12, 1999
Screening for mutations in the promoter and the coding region of the IGFBP1 and IGFBP3 genes in Silver-Russell syndrome patientsK Eggermann, H A Wollmann, J Tomiuk, et al.European Journal of Medical Genetics|April 11, 2006
(Epi)mutations in 11p15 significantly contribute to Silver-Russell syndrome: but are they generally involved in growth retardation?N Schönherr, E Meyer, K Eggermann, et al.Human Genetics|February 1, 1996
Trisomy of human chromosome 18: molecular studies on parental origin and cell stage of nondisjunctionT Eggermann, M M Nöthen, B Eiben, et al.Human Genetics|October 1, 1993
Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome)M M Nöthen, T Eggermann, J Erdmann, et al.Genetic Testing|January 15, 2002
Gene dosage analysis in Silver-Russell syndrome: use of quantitative competitive PCR and dual-color FISH to estimate the frequency of duplications in 7p11.2-p13S Mergenthaler, A Sharp, M B Ranke, et al.Journal of Medical Genetics|September 11, 1998
Paternally inherited deletion of CSH1 in a patient with Silver-Russell syndromeT Eggermann, K Eggermann, S Mergenthaler, et al.Pageof 7