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E Passarge

Showing results (101-110 of 151) with videos related to

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Human Molecular Genetics|December 1, 1994
Spectrum of small length germline mutations in the RB1 geneD R Lohmann, B Brandt, W Höpping, et al.
American Journal of Human Genetics|November 1, 1981
Functional deficiency of fibroblasts heterozygous for Bloom syndrome as specific manifestation of the primary defectC R Bartram, H W Rüdiger, U Schmidt-Preuss, et al.
Deutsche Medizinische Wochenschrift (1946)|October 27, 1972
[Identification of Y-chromosome anomalies using fluorescence microscopy. Study on 2 groups of prisoners as a contribution to the XYY problem]S Hellweg-Fründ, T Koske-Westphal, S Fuchs-Mecke, et al.
Der Pathologe|February 13, 2007
[Enzyme histochemistry of classical and ultrashort Hirschsprung's disease]E Bruder, L M Terracciano, E Passarge, et al.
American Journal of Human Genetics|May 1, 1996
The spectrum of RB1 germ-line mutations in hereditary retinoblastomaD R Lohmann, B Brandt, W Höpping, et al.
Lancet (London, England)|February 28, 1987
Early diagnosis in hereditary retinoblastoma by detection of molecular deletions at gene locusB Horsthemke, H J Barnert, V Greger, et al.
American Journal of Medical Genetics|December 31, 1997
Three brothers with mental and physical retardation, hydrocephalus, microcephaly, internal malformations, speech disorder, and facial anomalies: Mutchinick syndromeW Doerfler, D Wieczorek, G Gillessen-Kaesbach, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 11, 2001
[Analysis of a case of balanced chromosome translocation and phenotypic abnormality by fluorescence in situ hybridization]G Zhu, O Bartsch, M Wan, et al.
Human Genetics|October 1, 1994
Distinct RB1 gene mutations with low penetrance in hereditary retinoblastomaD R Lohmann, B Brandt, W Höpping, et al.
Human Genetics|July 1, 1987
Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locusB Horsthemke, V Greger, H J Barnert, et al.
Pageof 16

Showing results (101-110 of 151) with videos related to

Sort By:
Pageof 16
Human Molecular Genetics|December 1, 1994
Spectrum of small length germline mutations in the RB1 geneD R Lohmann, B Brandt, W Höpping, et al.
American Journal of Human Genetics|November 1, 1981
Functional deficiency of fibroblasts heterozygous for Bloom syndrome as specific manifestation of the primary defectC R Bartram, H W Rüdiger, U Schmidt-Preuss, et al.
Deutsche Medizinische Wochenschrift (1946)|October 27, 1972
[Identification of Y-chromosome anomalies using fluorescence microscopy. Study on 2 groups of prisoners as a contribution to the XYY problem]S Hellweg-Fründ, T Koske-Westphal, S Fuchs-Mecke, et al.
Der Pathologe|February 13, 2007
[Enzyme histochemistry of classical and ultrashort Hirschsprung's disease]E Bruder, L M Terracciano, E Passarge, et al.
American Journal of Human Genetics|May 1, 1996
The spectrum of RB1 germ-line mutations in hereditary retinoblastomaD R Lohmann, B Brandt, W Höpping, et al.
Lancet (London, England)|February 28, 1987
Early diagnosis in hereditary retinoblastoma by detection of molecular deletions at gene locusB Horsthemke, H J Barnert, V Greger, et al.
American Journal of Medical Genetics|December 31, 1997
Three brothers with mental and physical retardation, hydrocephalus, microcephaly, internal malformations, speech disorder, and facial anomalies: Mutchinick syndromeW Doerfler, D Wieczorek, G Gillessen-Kaesbach, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|April 11, 2001
[Analysis of a case of balanced chromosome translocation and phenotypic abnormality by fluorescence in situ hybridization]G Zhu, O Bartsch, M Wan, et al.
Human Genetics|October 1, 1994
Distinct RB1 gene mutations with low penetrance in hereditary retinoblastomaD R Lohmann, B Brandt, W Höpping, et al.
Human Genetics|July 1, 1987
Detection of submicroscopic deletions and a DNA polymorphism at the retinoblastoma locusB Horsthemke, V Greger, H J Barnert, et al.
Pageof 16