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Gynakologische Rundschau
|
January 1, 1989
[Genetic, biochemical and genomic prenatal diagnosis in genetic defects]
G Göretzlehner, G Machill, U Grimm, et al.
Zentralblatt Fur Gynakologie
|
January 1, 1975
[Prenatal brain damage in maternal, untreated phenylketonuria]
W H Peters, H Lubs, G Machill, et al.
Zeitschrift Fur Medizinische Laboratoriumsdiagnostik
|
January 1, 1988
[Modified treatment of DNA preparation for cultured amniotic fluid cells and chorionic tissue]
M Wehnert, U Kiessling, M Schütz, et al.
Zeitschrift Fur Arztliche Fortbildung
|
January 1, 1988
[Phenylketonuria from the current viewpoint]
G Seidlitz, G Machill, U Grimm, et al.
Human Heredity
|
January 1, 1991
Evidence supporting tight linkage of X-linked Emery-Dreifuss muscular dystrophy to the factor VIII:C gene
M Wehnert, G Machill, T Grimm, et al.
Das Deutsche Gesundheitswesen
|
October 14, 1971
[Routine early diagnosis of phenylketonuria using the Guthrie test in the GDR]
G Machill, K Schlenzka, G Cobet, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Mucopolysaccharidosis type II (Hunter syndrome): characterization of the iduronate-2-sulphatase in MPS II skin fibroblasts
L Petruschka, M Zschiesche, J Bielicki, et al.
Ceskoslovenska Pediatrie
|
May 1, 1985
[Metachromatic leukodystrophy with a familial incidence; prenatal diagnosis]
A Pijácková, Z Kaláb, G Machill, et al.
Acta Biologica Et Medica Germanica
|
January 1, 1975
[Determination of kynureninase activity in oligophrenic children with hereditary taint, before and after vitamin B6 treatment]
U Grimm, A Knapp, G Machill, et al.
European Journal of Pediatrics
|
January 1, 1994
Results of selective screening for inborn errors of metabolism in the former East Germany
G Machill, U Grimm, I Ahlbehrendt, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 41) with videos related to
Sort By:
Page
of 5
Gynakologische Rundschau
|
January 1, 1989
[Genetic, biochemical and genomic prenatal diagnosis in genetic defects]
G Göretzlehner, G Machill, U Grimm, et al.
Zentralblatt Fur Gynakologie
|
January 1, 1975
[Prenatal brain damage in maternal, untreated phenylketonuria]
W H Peters, H Lubs, G Machill, et al.
Zeitschrift Fur Medizinische Laboratoriumsdiagnostik
|
January 1, 1988
[Modified treatment of DNA preparation for cultured amniotic fluid cells and chorionic tissue]
M Wehnert, U Kiessling, M Schütz, et al.
Zeitschrift Fur Arztliche Fortbildung
|
January 1, 1988
[Phenylketonuria from the current viewpoint]
G Seidlitz, G Machill, U Grimm, et al.
Human Heredity
|
January 1, 1991
Evidence supporting tight linkage of X-linked Emery-Dreifuss muscular dystrophy to the factor VIII:C gene
M Wehnert, G Machill, T Grimm, et al.
Das Deutsche Gesundheitswesen
|
October 14, 1971
[Routine early diagnosis of phenylketonuria using the Guthrie test in the GDR]
G Machill, K Schlenzka, G Cobet, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1994
Mucopolysaccharidosis type II (Hunter syndrome): characterization of the iduronate-2-sulphatase in MPS II skin fibroblasts
L Petruschka, M Zschiesche, J Bielicki, et al.
Ceskoslovenska Pediatrie
|
May 1, 1985
[Metachromatic leukodystrophy with a familial incidence; prenatal diagnosis]
A Pijácková, Z Kaláb, G Machill, et al.
Acta Biologica Et Medica Germanica
|
January 1, 1975
[Determination of kynureninase activity in oligophrenic children with hereditary taint, before and after vitamin B6 treatment]
U Grimm, A Knapp, G Machill, et al.
European Journal of Pediatrics
|
January 1, 1994
Results of selective screening for inborn errors of metabolism in the former East Germany
G Machill, U Grimm, I Ahlbehrendt, et al.
Page
of 5