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E Passarge

Showing results (81-90 of 151) with videos related to

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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 syndromeD Wieczorek, G Gillessen-Kaesbach, S Plewa, et al.
Humangenetik|January 1, 1973
Maple syrup urine disease: rapid prenatal diagnosis by enzyme assayU 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 theoremU Langenbeck, T Grimm, H W Rüdiger, et al.
Journal of Medical Genetics|September 1, 1975
Alpha1-antitrypsin phenotypes in sex chromosome mosaicismF 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 phenotypeG 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- syndromeD 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 cultureH W Rüdiger, R Wolff, U Wendel, et al.
Pageof 16

Showing results (81-90 of 151) with videos related to

Sort By:
Pageof 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 syndromeD Wieczorek, G Gillessen-Kaesbach, S Plewa, et al.
Humangenetik|January 1, 1973
Maple syrup urine disease: rapid prenatal diagnosis by enzyme assayU 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 theoremU Langenbeck, T Grimm, H W Rüdiger, et al.
Journal of Medical Genetics|September 1, 1975
Alpha1-antitrypsin phenotypes in sex chromosome mosaicismF 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 phenotypeG 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- syndromeD 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 cultureH W Rüdiger, R Wolff, U Wendel, et al.
Pageof 16