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H Lubs

Showing results (31-40 of 47) with videos related to

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Acta Biologica Et Medica Germanica|January 1, 1975
[Histidine tolerance in low skin histidase activity]W H Peters, H Lubs, H Baumann, et al.
Acta Biologica Et Medica Germanica|January 1, 1974
[Simple microlitre-method for the determination of hypoxanthine-guanine-phosphoribosyl transferase activity in erythrocytes and skin fibroblasts]U Grimm, H Lubs, G Machill, et al.
Das Deutsche Gesundheitswesen|September 28, 1972
[Tryptophan metabolism studies in two siblings with oligophrenia and convulsions]U Grimm, A Knapp, K Schlenzka, et al.
Zentralblatt Fur Gynakologie|January 1, 1975
[Prenatal brain damage in maternal, untreated phenylketonuria]W H Peters, H Lubs, G Machill, et al.
Experimental and Clinical Endocrinology|August 1, 1987
Ketosis, serum carnitine and its precursor amino acids in normal and diabetic ethiopiansW H Peters, H Seim, H Löster, et al.
Neuropsychologia|August 1, 1993
Temporal lobe surface area measurements on MRI in normal and dyslexic readersA Kushch, K Gross-Glenn, B Jallad, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences|January 1, 1993
Adult familial dyslexia: a retrospective developmental and psychosocial profileE Feldman, B E Levin, H Lubs, et al.
Journal of Medical Genetics|June 3, 2006
Golabi-Ito-Hall syndrome results from a missense mutation in the WW domain of the PQBP1 geneH Lubs, F E Abidi, R Echeverri, et al.
American Journal of Medical Genetics|July 12, 1996
X-linked mental retardation with thin habitus, osteoporosis, and kyphoscoliosis: linkage to Xp21.3-p22.12J F Arena, C Schwartz, L Ouzts, et al.
American Journal of Medical Genetics|April 1, 1992
Fifth international workshop on fragile X and X-linked mental retardationJ L Mandel, R Hagerman, U Froster, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Acta Biologica Et Medica Germanica|January 1, 1975
[Histidine tolerance in low skin histidase activity]W H Peters, H Lubs, H Baumann, et al.
Acta Biologica Et Medica Germanica|January 1, 1974
[Simple microlitre-method for the determination of hypoxanthine-guanine-phosphoribosyl transferase activity in erythrocytes and skin fibroblasts]U Grimm, H Lubs, G Machill, et al.
Das Deutsche Gesundheitswesen|September 28, 1972
[Tryptophan metabolism studies in two siblings with oligophrenia and convulsions]U Grimm, A Knapp, K Schlenzka, et al.
Zentralblatt Fur Gynakologie|January 1, 1975
[Prenatal brain damage in maternal, untreated phenylketonuria]W H Peters, H Lubs, G Machill, et al.
Experimental and Clinical Endocrinology|August 1, 1987
Ketosis, serum carnitine and its precursor amino acids in normal and diabetic ethiopiansW H Peters, H Seim, H Löster, et al.
Neuropsychologia|August 1, 1993
Temporal lobe surface area measurements on MRI in normal and dyslexic readersA Kushch, K Gross-Glenn, B Jallad, et al.
The Journal of Neuropsychiatry and Clinical Neurosciences|January 1, 1993
Adult familial dyslexia: a retrospective developmental and psychosocial profileE Feldman, B E Levin, H Lubs, et al.
Journal of Medical Genetics|June 3, 2006
Golabi-Ito-Hall syndrome results from a missense mutation in the WW domain of the PQBP1 geneH Lubs, F E Abidi, R Echeverri, et al.
American Journal of Medical Genetics|July 12, 1996
X-linked mental retardation with thin habitus, osteoporosis, and kyphoscoliosis: linkage to Xp21.3-p22.12J F Arena, C Schwartz, L Ouzts, et al.
American Journal of Medical Genetics|April 1, 1992
Fifth international workshop on fragile X and X-linked mental retardationJ L Mandel, R Hagerman, U Froster, et al.
Pageof 5