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Schwinger

Showing results (621-630 of 849) with videos related to

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Human Mutation|January 1, 1993
Molecular basis of mucopolysaccharidosis type II: mutations in the iduronate-2-sulphatase geneJ J Hopwood, S Bunge, C P Morris, et al.
Bone Marrow Transplantation|August 5, 2000
Unrelated partially matched peripheral blood stem cell transplantation with highly purified CD34+ cells in a child with Wiskott-Aldrich syndromeW Schwinger, C Urban, H Lackner, et al.
Infection|April 27, 2000
Visceral manifestation of cat scratch disease in children. A consequence of altered immunological state?A Kahr, R Kerbl, K Gschwandtner, et al.
Journal of Pediatric Hematology/Oncology|January 10, 2009
Intracranial reparative giant cell granuloma secondary to cholesteatoma in a 15-year-old girlAndrea Moser, Karl M Hoffmann, Christian Walch, et al.
Zeitschrift Fur Gerontologie Und Geriatrie|March 16, 2021
[Medical specialist undertreatment in nursing home residents-Prevalence and extrapolation]Maike Schulz, Jonas Czwikla, Annika Schmidt, et al.
European Journal of Human Genetics : EJHG|June 5, 2014
Clinical utility gene card for: Angelman SyndromeKarin Buiting, Jill Clayton-Smith, Daniel J Driscoll, et al.
BMC Health Services Research|July 27, 2020
Claims data analysis of medical specialist utilization among nursing home residents and community-dwelling older peopleMaike Schulz, Chrysanthi Tsiasioti, Jonas Czwikla, et al.
Human Genetics|September 1, 1997
CAG repeat analyses in frozen and formalin-fixed tissues following primer extension preamplification for evaluation of mitotic instability of expanded SCA1 allelesC Zühlke, Y Hellenbroich, F Schaaff, et al.
European Journal of Human Genetics : EJHG|September 2, 2004
Extension of the mutation spectrum in Friedreich's ataxia: detection of an exon deletion and novel missense mutationsC H Zühlke, A Dalski, M Habeck, et al.
Human Mutation|February 22, 2002
Identification and in vitro expression of novel CDH23 mutations of patients with Usher syndrome type 1DBenigna von Brederlow, Hanno Bolz, Andreas Janecke, et al.
Pageof 85

Showing results (621-630 of 849) with videos related to

Sort By:
Pageof 85
Human Mutation|January 1, 1993
Molecular basis of mucopolysaccharidosis type II: mutations in the iduronate-2-sulphatase geneJ J Hopwood, S Bunge, C P Morris, et al.
Bone Marrow Transplantation|August 5, 2000
Unrelated partially matched peripheral blood stem cell transplantation with highly purified CD34+ cells in a child with Wiskott-Aldrich syndromeW Schwinger, C Urban, H Lackner, et al.
Infection|April 27, 2000
Visceral manifestation of cat scratch disease in children. A consequence of altered immunological state?A Kahr, R Kerbl, K Gschwandtner, et al.
Journal of Pediatric Hematology/Oncology|January 10, 2009
Intracranial reparative giant cell granuloma secondary to cholesteatoma in a 15-year-old girlAndrea Moser, Karl M Hoffmann, Christian Walch, et al.
Zeitschrift Fur Gerontologie Und Geriatrie|March 16, 2021
[Medical specialist undertreatment in nursing home residents-Prevalence and extrapolation]Maike Schulz, Jonas Czwikla, Annika Schmidt, et al.
European Journal of Human Genetics : EJHG|June 5, 2014
Clinical utility gene card for: Angelman SyndromeKarin Buiting, Jill Clayton-Smith, Daniel J Driscoll, et al.
BMC Health Services Research|July 27, 2020
Claims data analysis of medical specialist utilization among nursing home residents and community-dwelling older peopleMaike Schulz, Chrysanthi Tsiasioti, Jonas Czwikla, et al.
Human Genetics|September 1, 1997
CAG repeat analyses in frozen and formalin-fixed tissues following primer extension preamplification for evaluation of mitotic instability of expanded SCA1 allelesC Zühlke, Y Hellenbroich, F Schaaff, et al.
European Journal of Human Genetics : EJHG|September 2, 2004
Extension of the mutation spectrum in Friedreich's ataxia: detection of an exon deletion and novel missense mutationsC H Zühlke, A Dalski, M Habeck, et al.
Human Mutation|February 22, 2002
Identification and in vitro expression of novel CDH23 mutations of patients with Usher syndrome type 1DBenigna von Brederlow, Hanno Bolz, Andreas Janecke, et al.
Pageof 85