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Klinische Padiatrie|January 1, 1993
[Development of brain atrophy, therapy and therapy monitoring in glutaric aciduria type I (glutaryl-CoA dehydrogenase deficiency)]B Lawrenz-Wolf, K P Herberg, G F Hoffmann, et al.Human Mutation|July 29, 1999
Identification of 9 novel FBN1 mutations in German patients with Marfan syndromeA A El-Aleem, M Karck, A Haverich, et al.Cancer Genetics and Cytogenetics|February 1, 1989
Characterization of rearranged Y chromosomes in human testicular tumor cell linesJ Arnemann, G Gradl, J Casper, et al.Human Mutation|April 29, 1998
A new missense substitution at a mutational hot spot of the androgen receptor in siblings with complete androgen insensitivity syndromeT Dörk, F Schnieders, S Jakubiczka, et al.Human Genetics|February 1, 1991
Characterisation of a Xp21 microdeletion syndrome in a 2-year-old boy with muscular dystrophy, glycerol kinase deficiency and adrenal hypoplasia congenitaM Stuhrmann, H Heilbronner, A Reis, et al.Human Genetics|January 1, 1985
An estimate of unique DNA sequence heterozygosity in the human genomeD N Cooper, B A Smith, H J Cooke, et al.Dalton Transactions (Cambridge, England : 2003)|December 28, 2020
Lipophilic Re(CO)3pyca complexes for Mid-IR imaging applicationsBriana R Schrage, Baylee R Frisinger, Sarah J Schmidtke Sobeck, et al.Human Genetics|June 1, 1991
A sterile male with 45,X0 and a Y;22 translocationJ Arnemann, S Schnittger, G K Hinkel, et al.Journal of Inherited Metabolic Disease|March 1, 1997
Decreased platelet membrane anisotropy in patients with adrenoleukodystrophy treated with erucic acid (22:1)-rich triglyceridesS Stöckler, C Opper, A Greinacher, et al.Respiration Physiology|January 4, 1998
Intracellular signal pathways controlling respiratory neuronsD W Richter, P M Lalley, O Pierrefiche, et al.Pageof 33