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G Seidlitz

Showing results (41-50 of 48) with videos related to

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European Journal of Pediatrics|January 1, 1994
Results of selective screening for inborn errors of metabolism in the former East GermanyG Machill, U Grimm, I Ahlbehrendt, et al.
Zeitschrift Fur Arztliche Fortbildung|January 1, 1988
[Prenatal biochemical diagnosis in genetically-induced metabolic diseases]G Machill, G Seidlitz, U Grimm, et al.
Kinderarztliche Praxis|December 1, 1989
[A staged plan for laboratory diagnosis of hereditary metabolic diseases]H Zöllner, W Tittelbach-Helmrich, N Bannert, et al.
American Journal of Obstetrics and Gynecology|April 16, 1999
Undiagnosed maternal phenylketonuria: the need for prenatal selective screening or case findingW B Hanley, L D Platt, R P Bachman, et al.
Human Molecular Genetics|June 1, 1992
Molecular analysis of patients with Hunter syndrome: implication of a region prone to structural alterations within the IDS geneM L Steén-Bondeson, N Dahl, T Tönnesen, et al.
Kinderarztliche Praxis|May 1, 1978
[Intersexual organ abnormalities in childhood. III. Sex assignment and principles of medical treatment]L Pelz, K R Sandig, W Hoepffner, et al.
Kinderarztliche Praxis|January 1, 1978
[Intersexual organ malformations in childhood. II. Frequency and clinical aspects, including differential diagnosis]K R Sandig, L Pelz, W Hoepffner, et al.
Kinderarztliche Praxis|December 1, 1977
[Intersexual organ malformations in childhood. I. Definition, classification, problems and diagnosis]K R Sandig, L Pelz, W Hoepffner, et al.
Pageof 5

Showing results (41-50 of 48) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 48 results.
European Journal of Pediatrics|January 1, 1994
Results of selective screening for inborn errors of metabolism in the former East GermanyG Machill, U Grimm, I Ahlbehrendt, et al.
Zeitschrift Fur Arztliche Fortbildung|January 1, 1988
[Prenatal biochemical diagnosis in genetically-induced metabolic diseases]G Machill, G Seidlitz, U Grimm, et al.
Kinderarztliche Praxis|December 1, 1989
[A staged plan for laboratory diagnosis of hereditary metabolic diseases]H Zöllner, W Tittelbach-Helmrich, N Bannert, et al.
American Journal of Obstetrics and Gynecology|April 16, 1999
Undiagnosed maternal phenylketonuria: the need for prenatal selective screening or case findingW B Hanley, L D Platt, R P Bachman, et al.
Human Molecular Genetics|June 1, 1992
Molecular analysis of patients with Hunter syndrome: implication of a region prone to structural alterations within the IDS geneM L Steén-Bondeson, N Dahl, T Tönnesen, et al.
Kinderarztliche Praxis|May 1, 1978
[Intersexual organ abnormalities in childhood. III. Sex assignment and principles of medical treatment]L Pelz, K R Sandig, W Hoepffner, et al.
Kinderarztliche Praxis|January 1, 1978
[Intersexual organ malformations in childhood. II. Frequency and clinical aspects, including differential diagnosis]K R Sandig, L Pelz, W Hoepffner, et al.
Kinderarztliche Praxis|December 1, 1977
[Intersexual organ malformations in childhood. I. Definition, classification, problems and diagnosis]K R Sandig, L Pelz, W Hoepffner, et al.
Pageof 5