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Acta Biologica Et Medica Germanica
|
January 1, 1975
[Alpha-L-iduronidase activity in fibroblasts of patients with Hurler syndrome]
G Stareprawo, U Grimm, G Machill, et al.
Padiatrie Und Grenzgebiete
|
January 1, 1982
[Tryptophan metabolism in infants with phenylketonuria]
P Bührdel, U Grimm, S Wässer, et al.
Dermatologische Monatschrift
|
December 1, 1976
[Generalized circumscribed scleroderma and phenylketonuric metabolic changes in a girl whose mother was irradiated because of abdominal carcinoma]
U Haufe, U Grimm, K Herrmann, et al.
Thrombosis and Haemostasis
|
April 26, 2000
No evidence for the CD31 C/G gene polymorphism as an independent risk factor of coronary heart disease
A Gardemann, A Knapp, N Katz, et al.
Human Genetics
|
January 1, 1983
Reliability of the Tønnesen technique for the identification of Hunter carriers
L Petruschka, G Machill, M Wehnert, et al.
Zeitschrift Fur Urologie Und Nephrologie
|
May 1, 1988
[Studies on tryptophan metabolism in calcium oxalate urolithiasis]
U Grimm, I Steinhauser, K Wulff, et al.
Biomedica Biochimica Acta
|
January 1, 1990
Tryptophan metabolic studies in patients with presenile cataracts
U Grimm, A Knapp, G Seidlitz, et al.
Advances in Experimental Medicine and Biology
|
January 3, 2012
Patient provider communication and reproductive health
Caprice A Knapp, Gwendolyn P Quinn, Deborah Rapalo, et al.
Gastroenterologisches Journal : Organ Der Gesellschaft Fur Gastroenterologie Der DDR
|
January 1, 1990
[The HLA and protease inhibitor (Pi) system in erythropoietic (hepatic) protoporphyria. Family studies]
E Köstler, B Gebhardt, A Knapp, et al.
Experimental and Clinical Immunogenetics
|
November 14, 1998
The major histocompatibility complex and mate choice: inbreeding avoidance and selection of good genes
B Grob, L A Knapp, R D Martin, et al.
Page
of 55
Search research articles
Search
Showing results (221-230 of 544) with videos related to
Sort By:
Page
of 55
Acta Biologica Et Medica Germanica
|
January 1, 1975
[Alpha-L-iduronidase activity in fibroblasts of patients with Hurler syndrome]
G Stareprawo, U Grimm, G Machill, et al.
Padiatrie Und Grenzgebiete
|
January 1, 1982
[Tryptophan metabolism in infants with phenylketonuria]
P Bührdel, U Grimm, S Wässer, et al.
Dermatologische Monatschrift
|
December 1, 1976
[Generalized circumscribed scleroderma and phenylketonuric metabolic changes in a girl whose mother was irradiated because of abdominal carcinoma]
U Haufe, U Grimm, K Herrmann, et al.
Thrombosis and Haemostasis
|
April 26, 2000
No evidence for the CD31 C/G gene polymorphism as an independent risk factor of coronary heart disease
A Gardemann, A Knapp, N Katz, et al.
Human Genetics
|
January 1, 1983
Reliability of the Tønnesen technique for the identification of Hunter carriers
L Petruschka, G Machill, M Wehnert, et al.
Zeitschrift Fur Urologie Und Nephrologie
|
May 1, 1988
[Studies on tryptophan metabolism in calcium oxalate urolithiasis]
U Grimm, I Steinhauser, K Wulff, et al.
Biomedica Biochimica Acta
|
January 1, 1990
Tryptophan metabolic studies in patients with presenile cataracts
U Grimm, A Knapp, G Seidlitz, et al.
Advances in Experimental Medicine and Biology
|
January 3, 2012
Patient provider communication and reproductive health
Caprice A Knapp, Gwendolyn P Quinn, Deborah Rapalo, et al.
Gastroenterologisches Journal : Organ Der Gesellschaft Fur Gastroenterologie Der DDR
|
January 1, 1990
[The HLA and protease inhibitor (Pi) system in erythropoietic (hepatic) protoporphyria. Family studies]
E Köstler, B Gebhardt, A Knapp, et al.
Experimental and Clinical Immunogenetics
|
November 14, 1998
The major histocompatibility complex and mate choice: inbreeding avoidance and selection of good genes
B Grob, L A Knapp, R D Martin, et al.
Page
of 55