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K Eggermann

Showing results (1-10 of 33) with videos related to

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Deutsche Krankenpflegezeitschrift|November 1, 1992
[Use of computers in nursing schools]K Eggermann
Journal of Medical Genetics|May 19, 2001
Uniparental isodisomy for paternal 2p and maternal 2q in a phenotypically normal female with two isochromosomes, i(2p) and i(2q)B Albrecht, S Mergenthaler, K Eggermann, et al.
Orvosi Hetilap|August 10, 2001
[Uniparental disomy 7 in the pathogenesis of Silver-Russell syndrome]S Mergenthaler, M Dobos, H Wollmann, et al.
American Journal of Medical Genetics|May 8, 2000
Rare case of De Novo interstitial deletion 2q13q21: clinical, cytogenetic, and molecular studiesK Eggermann, A Dufke, H Enders, et al.
Clinical Genetics|March 21, 2002
Segmental uniparental disomy of 7q31-qter is rare in Silver-Russell syndromeT Eggermann, S Mergenthaler, K Eggermann, et al.
Cytogenetics and Cell Genetics|February 15, 2001
A second case of inv(4)pat with both recombinants in the offspring: rec dup(4q) in a girl with Wolf-Hirschhorn syndrome and rec dup(4p)A Dufke, K Eggermann, S Balg, et al.
Clinical Genetics|May 22, 2001
IRS1 and GRB2 as members of the IGF signal transduction pathway are not associated with intrauterine growth retardation and Silver-Russell syndromeT Eggermann, P Kloos, S Mergenthaler, 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.
Journal of Medical Genetics|January 11, 2000
Exclusion of a disease relevant role of PAX4 in the aetiology of Silver-Russell syndrome: screening for mutations and determination of imprinting statusS Mergenthaler, K Eggermann, J Tomiuk, 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.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Deutsche Krankenpflegezeitschrift|November 1, 1992
[Use of computers in nursing schools]K Eggermann
Journal of Medical Genetics|May 19, 2001
Uniparental isodisomy for paternal 2p and maternal 2q in a phenotypically normal female with two isochromosomes, i(2p) and i(2q)B Albrecht, S Mergenthaler, K Eggermann, et al.
Orvosi Hetilap|August 10, 2001
[Uniparental disomy 7 in the pathogenesis of Silver-Russell syndrome]S Mergenthaler, M Dobos, H Wollmann, et al.
American Journal of Medical Genetics|May 8, 2000
Rare case of De Novo interstitial deletion 2q13q21: clinical, cytogenetic, and molecular studiesK Eggermann, A Dufke, H Enders, et al.
Clinical Genetics|March 21, 2002
Segmental uniparental disomy of 7q31-qter is rare in Silver-Russell syndromeT Eggermann, S Mergenthaler, K Eggermann, et al.
Cytogenetics and Cell Genetics|February 15, 2001
A second case of inv(4)pat with both recombinants in the offspring: rec dup(4q) in a girl with Wolf-Hirschhorn syndrome and rec dup(4p)A Dufke, K Eggermann, S Balg, et al.
Clinical Genetics|May 22, 2001
IRS1 and GRB2 as members of the IGF signal transduction pathway are not associated with intrauterine growth retardation and Silver-Russell syndromeT Eggermann, P Kloos, S Mergenthaler, 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.
Journal of Medical Genetics|January 11, 2000
Exclusion of a disease relevant role of PAX4 in the aetiology of Silver-Russell syndrome: screening for mutations and determination of imprinting statusS Mergenthaler, K Eggermann, J Tomiuk, 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.
Pageof 4