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U Langenbeck

Showing results (11-20 of 68) with videos related to

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Metabolism: Clinical and Experimental|January 1, 1985
Serum branched chain amino and keto acid response to fasting in humansP Schauder, L Herbertz, U Langenbeck
American Journal of Medical Genetics|October 1, 1985
Familial microtia, meatal atresia, and conductive deafness in three siblingsM Schmid, M Schröder, U Langenbeck
Analytical Biochemistry|July 1, 1989
Monitoring of phenylketonuria: a colorimetric method for the determination of plasma phenylalanine using L-phenylalanine dehydrogenaseU Wendel, W Hummel, U Langenbeck
Cytogenetics and Cell Genetics|February 15, 2001
Parent-offspring resemblance of palmar and plantar dermatoglyphic patterns in Down syndromeU Langenbeck, G Herzberger, S Kümmerle
Zeitschrift Fur Geburtshilfe Und Perinatologie|November 1, 1991
[Fryns syndrome--pre and postnatal diagnosis]U Dix, U Beudt, U Langenbeck
Pediatric Research|January 1, 1989
Interrelation between the metabolism of L-isoleucine and L-allo-isoleucine in patients with maple syrup urine diseaseU Wendel, U Langenbeck, J W Seakins
Biomedical Mass Spectrometry|March 1, 1983
Quantitative gas chromatographic mass spectrometric determination of mandelic acid in blood plasma. Comparison of deuterated and homologous internal standardsH Luthe, H Ludwig-Köhn, U Langenbeck
Journal of Inherited Metabolic Disease|January 1, 1992
A synopsis of the unconjugated acidic transamination metabolites of phenylalanine in phenylketonuriaU Langenbeck, A Behbehani, A Mench-Hoinowski
American Journal of Medical Genetics|January 1, 1988
Skeletal anomalies in trisomy 21 as an example of amplified developmental instability in chromosome disorders: a histological study of the feet of 21 mid-trimester fetuses with trisomy 21E Blum-Hoffmann, H Rehder, U Langenbeck
American Journal of Human Genetics|May 1, 1980
Genetics of the apolipoprotein E system in manG Utermann, U Langenbeck, U Beisiegel, et al.
Pageof 7

Showing results (11-20 of 68) with videos related to

Sort By:
Pageof 7
Metabolism: Clinical and Experimental|January 1, 1985
Serum branched chain amino and keto acid response to fasting in humansP Schauder, L Herbertz, U Langenbeck
American Journal of Medical Genetics|October 1, 1985
Familial microtia, meatal atresia, and conductive deafness in three siblingsM Schmid, M Schröder, U Langenbeck
Analytical Biochemistry|July 1, 1989
Monitoring of phenylketonuria: a colorimetric method for the determination of plasma phenylalanine using L-phenylalanine dehydrogenaseU Wendel, W Hummel, U Langenbeck
Cytogenetics and Cell Genetics|February 15, 2001
Parent-offspring resemblance of palmar and plantar dermatoglyphic patterns in Down syndromeU Langenbeck, G Herzberger, S Kümmerle
Zeitschrift Fur Geburtshilfe Und Perinatologie|November 1, 1991
[Fryns syndrome--pre and postnatal diagnosis]U Dix, U Beudt, U Langenbeck
Pediatric Research|January 1, 1989
Interrelation between the metabolism of L-isoleucine and L-allo-isoleucine in patients with maple syrup urine diseaseU Wendel, U Langenbeck, J W Seakins
Biomedical Mass Spectrometry|March 1, 1983
Quantitative gas chromatographic mass spectrometric determination of mandelic acid in blood plasma. Comparison of deuterated and homologous internal standardsH Luthe, H Ludwig-Köhn, U Langenbeck
Journal of Inherited Metabolic Disease|January 1, 1992
A synopsis of the unconjugated acidic transamination metabolites of phenylalanine in phenylketonuriaU Langenbeck, A Behbehani, A Mench-Hoinowski
American Journal of Medical Genetics|January 1, 1988
Skeletal anomalies in trisomy 21 as an example of amplified developmental instability in chromosome disorders: a histological study of the feet of 21 mid-trimester fetuses with trisomy 21E Blum-Hoffmann, H Rehder, U Langenbeck
American Journal of Human Genetics|May 1, 1980
Genetics of the apolipoprotein E system in manG Utermann, U Langenbeck, U Beisiegel, et al.
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