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U Langenbeck

Showing results (61-70 of 68) with videos related to

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Muscle & Nerve|March 1, 1983
Mallory body-like inclusions in a hereditary congenital neuromuscular diseaseA Fidzianska, H H Goebel, M Osborn, et al.
Human Genetics|January 1, 1984
Restriction fragment length polymorphisms at the human parathyroid hormone gene locusJ Schmidtke, B Pape, U Krengel, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 1, 1978
Correlations between branched-chain amino acids and branched-chain alpha-keto acids in blood in maple syrup urine diseaseU Langenbeck, U Wendel, A Mench-Hoinowski, et al.
European Journal of Pediatrics|February 1, 1982
A familial progressive neurodegenerative disease with 2-oxoglutaric aciduriaA Kohlschütter, A Behbehani, U Langenbeck, et al.
European Journal of Pediatrics|November 1, 1984
Mitochondrial myopathy with lactic acidosis and deficient activity of muscle succinate cytochrome-c-oxidoreductaseA W Behbehani, H Goebel, G Osse, et al.
European Journal of Pediatrics|June 1, 1991
Sphingolipid activator protein 1 deficiency in metachromatic leucodystrophy with normal arylsulphatase A activity. A clinical, morphological, biochemical, and immunological studyW Schlote, K Harzer, H Christomanou, et al.
Clinical Genetics|July 1, 1986
Dermatoglyphic peculiarities in families with X-linked mental retardation and fragile site Xq27: a collaborative studyA Rodewald, U Froster-Iskenius, E Käb, et al.
American Journal of Medical Genetics|January 1, 1981
The dup(3q) syndrome: report of eight cases and review of the literatureP Steinbach, W N Adkins, H Caspar, et al.
Pageof 7

Showing results (61-70 of 68) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 68 results.
Muscle & Nerve|March 1, 1983
Mallory body-like inclusions in a hereditary congenital neuromuscular diseaseA Fidzianska, H H Goebel, M Osborn, et al.
Human Genetics|January 1, 1984
Restriction fragment length polymorphisms at the human parathyroid hormone gene locusJ Schmidtke, B Pape, U Krengel, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 1, 1978
Correlations between branched-chain amino acids and branched-chain alpha-keto acids in blood in maple syrup urine diseaseU Langenbeck, U Wendel, A Mench-Hoinowski, et al.
European Journal of Pediatrics|February 1, 1982
A familial progressive neurodegenerative disease with 2-oxoglutaric aciduriaA Kohlschütter, A Behbehani, U Langenbeck, et al.
European Journal of Pediatrics|November 1, 1984
Mitochondrial myopathy with lactic acidosis and deficient activity of muscle succinate cytochrome-c-oxidoreductaseA W Behbehani, H Goebel, G Osse, et al.
European Journal of Pediatrics|June 1, 1991
Sphingolipid activator protein 1 deficiency in metachromatic leucodystrophy with normal arylsulphatase A activity. A clinical, morphological, biochemical, and immunological studyW Schlote, K Harzer, H Christomanou, et al.
Clinical Genetics|July 1, 1986
Dermatoglyphic peculiarities in families with X-linked mental retardation and fragile site Xq27: a collaborative studyA Rodewald, U Froster-Iskenius, E Käb, et al.
American Journal of Medical Genetics|January 1, 1981
The dup(3q) syndrome: report of eight cases and review of the literatureP Steinbach, W N Adkins, H Caspar, et al.
Pageof 7