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K Eggermann

Showing results (11-20 of 33) with videos related to

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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.
Revue Neurologique|July 7, 2021
Recurrent abdominal pain in hereditary sensory autonomic neuropathy type II (HSAN-II)H Alkaissi, E Al-Sibahee, H Baher, et al.
Nature Genetics|June 1, 1996
CNTF and psychiatric disordersM M Nöthen, S Cichon, K Eggermann, 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.
Annales De Genetique|May 4, 2001
Origin of uniparental disomy 6: presentation of a new case and review on the literatureT Eggermann, W Marg, S Mergenthaler, et al.
Clinical Genetics|December 12, 2007
Use of multiplex ligation-dependent probe amplification increases the detection rate for 11p15 epigenetic alterations in Silver-Russell syndromeT Eggermann, N Schönherr, K Eggermann, et al.
Human Genetics|September 1, 1997
Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomyT Eggermann, H A Wollmann, R Kuner, et al.
Clinical Genetics|February 9, 2000
Search for uniparental disomy 14 in balanced Robertsonian translocation carriersT Eggermann, M Wolf, C Spaich, et al.
Genes|December 23, 2022
Clonal Elimination of the Pathogenic Allele as Diagnostic Pitfall in <i>SAMD9L</i>-Associated NeuropathyK Eggermann, R Meyer, M Begemann, et al.
Journal of Medical Genetics|May 3, 2005
Is maternal duplication of 11p15 associated with Silver-Russell syndrome?T Eggermann, E Meyer, C Obermann, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
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.
Revue Neurologique|July 7, 2021
Recurrent abdominal pain in hereditary sensory autonomic neuropathy type II (HSAN-II)H Alkaissi, E Al-Sibahee, H Baher, et al.
Nature Genetics|June 1, 1996
CNTF and psychiatric disordersM M Nöthen, S Cichon, K Eggermann, 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.
Annales De Genetique|May 4, 2001
Origin of uniparental disomy 6: presentation of a new case and review on the literatureT Eggermann, W Marg, S Mergenthaler, et al.
Clinical Genetics|December 12, 2007
Use of multiplex ligation-dependent probe amplification increases the detection rate for 11p15 epigenetic alterations in Silver-Russell syndromeT Eggermann, N Schönherr, K Eggermann, et al.
Human Genetics|September 1, 1997
Molecular studies in 37 Silver-Russell syndrome patients: frequency and etiology of uniparental disomyT Eggermann, H A Wollmann, R Kuner, et al.
Clinical Genetics|February 9, 2000
Search for uniparental disomy 14 in balanced Robertsonian translocation carriersT Eggermann, M Wolf, C Spaich, et al.
Genes|December 23, 2022
Clonal Elimination of the Pathogenic Allele as Diagnostic Pitfall in <i>SAMD9L</i>-Associated NeuropathyK Eggermann, R Meyer, M Begemann, et al.
Journal of Medical Genetics|May 3, 2005
Is maternal duplication of 11p15 associated with Silver-Russell syndrome?T Eggermann, E Meyer, C Obermann, et al.
Pageof 4