Search research articles
Contact Us
Filters
Showing results (81-90 of 151) with videos related to
Page
of 16
Sort By:
Clinical Genetics
|
February 1, 1996
Microcephaly, seizures, genital hypoplasia, and abnormalities of the hands and feet in a 4-year-old boy with possible Wiedemann syndrome
D Wieczorek, G Gillessen-Kaesbach, S Plewa, et al.
Humangenetik
|
January 1, 1973
Maple syrup urine disease: rapid prenatal diagnosis by enzyme assay
U Wendel, H W Rüdiger, E Passarge, et al.
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie
|
October 1, 1972
[Aspects of metabolic correction in cells with pathologically increased mucopolysaccharide storage]
U Wendel, W Wöhler, H W Rüdiger, et al.
Humangenetik
|
January 1, 1975
Heterozygote tests and genetic counseling in maple syrup urine disease: an application of Baye's theorem
U Langenbeck, T Grimm, H W Rüdiger, et al.
Journal of Medical Genetics
|
September 1, 1975
Alpha1-antitrypsin phenotypes in sex chromosome mosaicism
F Kueppers, P O'Brien, E Passarge, et al.
American Journal of Medical Genetics
|
April 10, 1995
Further patient with Angelman syndrome due to paternal disomy of chromosome 15 and a milder phenotype
G Gillessen-Kaesbach, B Albrecht, E Passarge, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft
|
April 1, 1997
[Molecular genetics and diagnosis of retinoblastoma. Significance for ophthalmologic practice]
D R Lohmann, B Brandt, E Passarge, et al.
The Journal of Pediatrics
|
January 1, 1970
Human chromosomal deletion: two patients with the 4p- syndrome
D Arias, E Passarge, M A Engle, et al.
Deutsche Medizinische Wochenschrift (1946)
|
January 25, 1974
[Diseases caused by genetic defects in lysosomal muco-polysaccharide-catabolism. Mucopolysaccharidoses]
E Passarge, U Wendel, W Wöhler, et al.
Humangenetik
|
April 24, 1974
Enhancement of amniotic fluid cell growth in culture
H W Rüdiger, R Wolff, U Wendel, et al.
Page
of 16
Search research articles
Search
Showing results (81-90 of 151) with videos related to
Sort By:
Page
of 16
Clinical Genetics
|
February 1, 1996
Microcephaly, seizures, genital hypoplasia, and abnormalities of the hands and feet in a 4-year-old boy with possible Wiedemann syndrome
D Wieczorek, G Gillessen-Kaesbach, S Plewa, et al.
Humangenetik
|
January 1, 1973
Maple syrup urine disease: rapid prenatal diagnosis by enzyme assay
U Wendel, H W Rüdiger, E Passarge, et al.
Hoppe-Seyler'S Zeitschrift Fur Physiologische Chemie
|
October 1, 1972
[Aspects of metabolic correction in cells with pathologically increased mucopolysaccharide storage]
U Wendel, W Wöhler, H W Rüdiger, et al.
Humangenetik
|
January 1, 1975
Heterozygote tests and genetic counseling in maple syrup urine disease: an application of Baye's theorem
U Langenbeck, T Grimm, H W Rüdiger, et al.
Journal of Medical Genetics
|
September 1, 1975
Alpha1-antitrypsin phenotypes in sex chromosome mosaicism
F Kueppers, P O'Brien, E Passarge, et al.
American Journal of Medical Genetics
|
April 10, 1995
Further patient with Angelman syndrome due to paternal disomy of chromosome 15 and a milder phenotype
G Gillessen-Kaesbach, B Albrecht, E Passarge, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft
|
April 1, 1997
[Molecular genetics and diagnosis of retinoblastoma. Significance for ophthalmologic practice]
D R Lohmann, B Brandt, E Passarge, et al.
The Journal of Pediatrics
|
January 1, 1970
Human chromosomal deletion: two patients with the 4p- syndrome
D Arias, E Passarge, M A Engle, et al.
Deutsche Medizinische Wochenschrift (1946)
|
January 25, 1974
[Diseases caused by genetic defects in lysosomal muco-polysaccharide-catabolism. Mucopolysaccharidoses]
E Passarge, U Wendel, W Wöhler, et al.
Humangenetik
|
April 24, 1974
Enhancement of amniotic fluid cell growth in culture
H W Rüdiger, R Wolff, U Wendel, et al.
Page
of 16