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N Horn

Showing results (81-90 of 150) with videos related to

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Annals of Neurology|October 17, 2001
Multisystem disorder associated with a missense mutation in the mitochondrial cytochrome b geneF Wibrand, K Ravn, M Schwartz, et al.
Seminars in Cutaneous Medicine and Surgery|June 29, 2010
Clinical update on graft-versus-host disease in childrenDeborah S Goddard, Biljana N Horn, Timothy H McCalmont, et al.
American Journal of Human Genetics|May 1, 1992
Multipoint linkage analysis in Menkes diseaseT Tønnesen, A Petterson, T A Kruse, et al.
Human Genetics|March 1, 1992
Mapping of the Menkes locus to Xq13.3 distal to the X-inactivation center by an intrachromosomal insertion of the segment Xq13.3-q21.2Z Tümer, N Tommerup, T Tønnesen, et al.
Clinical Genetics|December 18, 2002
X-linked recessive Menkes disease: identification of partial gene deletions in affected malesL Poulsen, N Horn, H Heilstrup, et al.
Biochimica Et Biophysica Acta|August 9, 2011
Characterization of a potent antimicrobial lipopeptide via coarse-grained molecular dynamicsJoshua N Horn, Jesse D Sengillo, Dejun Lin, et al.
Human Genetics|January 1, 1983
Evidence that the Menkes locus maps on proximal XpT F Wienker, P Wieacker, H J Cooke, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndromeK Ravn, F Wibrand, F J Hansen, et al.
Biochemistry|December 20, 1983
Alterations in copper and collagen metabolism in the Menkes syndrome and a new subtype of the Ehlers-Danlos syndromeL Peltonen, H Kuivaniemi, A Palotie, et al.
Nature Genetics|January 1, 1996
Early copper-histidine treatment for Menkes diseaseZ Tümer, N Horn, T Tønnesen, et al.
Pageof 15

Showing results (81-90 of 150) with videos related to

Sort By:
Pageof 15
Annals of Neurology|October 17, 2001
Multisystem disorder associated with a missense mutation in the mitochondrial cytochrome b geneF Wibrand, K Ravn, M Schwartz, et al.
Seminars in Cutaneous Medicine and Surgery|June 29, 2010
Clinical update on graft-versus-host disease in childrenDeborah S Goddard, Biljana N Horn, Timothy H McCalmont, et al.
American Journal of Human Genetics|May 1, 1992
Multipoint linkage analysis in Menkes diseaseT Tønnesen, A Petterson, T A Kruse, et al.
Human Genetics|March 1, 1992
Mapping of the Menkes locus to Xq13.3 distal to the X-inactivation center by an intrachromosomal insertion of the segment Xq13.3-q21.2Z Tümer, N Tommerup, T Tønnesen, et al.
Clinical Genetics|December 18, 2002
X-linked recessive Menkes disease: identification of partial gene deletions in affected malesL Poulsen, N Horn, H Heilstrup, et al.
Biochimica Et Biophysica Acta|August 9, 2011
Characterization of a potent antimicrobial lipopeptide via coarse-grained molecular dynamicsJoshua N Horn, Jesse D Sengillo, Dejun Lin, et al.
Human Genetics|January 1, 1983
Evidence that the Menkes locus maps on proximal XpT F Wienker, P Wieacker, H J Cooke, et al.
European Journal of Human Genetics : EJHG|January 10, 2002
An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndromeK Ravn, F Wibrand, F J Hansen, et al.
Biochemistry|December 20, 1983
Alterations in copper and collagen metabolism in the Menkes syndrome and a new subtype of the Ehlers-Danlos syndromeL Peltonen, H Kuivaniemi, A Palotie, et al.
Nature Genetics|January 1, 1996
Early copper-histidine treatment for Menkes diseaseZ Tümer, N Horn, T Tønnesen, et al.
Pageof 15