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Biochimica Et Biophysica Acta|December 14, 1976
Determination of Triton X-100 binding to membrane proteins by polyacrylamide gel electrophoresisE FriesGenetic Counseling (Geneva, Switzerland)|January 1, 1995
A nine-month-old boy with microcephaly, cataracts, intracerebral calcifications and dysmorphic signs: an additional observation of an autosomal recessive congenital infection-like syndrome?D Wieczorek, G Gillessen-Kaesbach, E PassargeCancer Genetics and Cytogenetics|January 1, 1989
Mechanism of i(6p) formation in retinoblastoma tumor cellsB Horsthemke, V Greger, R Becher, et al.Annals of Human Genetics|July 1, 1976
Chromatid exchanges in ataxia telangiectasia, Bloom syndrome, Werner syndrome, and xeroderma pigmentosumC R Bartram, T Koske-Westphal, E PassargeHuman Genetics|February 15, 1979
Frequency of sister chromatid exchanges in Bloom syndrome fibroblasts reduced by cocultivation with normal cellsC R Bartram, H W Rüdiger, E PassargeHealth Care Financing Review|February 3, 1991
Comparing case-mix systems for nursing home paymentB E FriesClinical 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, 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.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.Pageof 31