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D R Lohmann

Showing results (11-20 of 25) with videos related to

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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.
Journal of Medical Genetics|December 14, 2004
Recurrent deletion of a region containing exon 24 of the RB1 gene caused by non-homologous recombination between a LINE-1HS and MER21B elementP Albrecht, J Bode, K Buiting, et al.
Virchows Archiv. B, Cell Pathology Including Molecular Pathology|January 1, 1993
Identification of p53 gene mutations in gastrointestinal and pancreatic carcinoids by nonradioisotopic SSCAD R Lohmann, A Funk, H P Niedermeyer, et al.
Journal of Medical Genetics|June 1, 1995
Identification of RB1 germline mutations in Argentinian families with sporadic bilateral retinoblastomaI Szijan, D R Lohmann, D L Parma, et al.
European Journal of Human Genetics : EJHG|September 26, 2001
Multiple lipomas linked to an RB1 gene mutation in a large pedigree with low penetrance retinoblastomaM Genuardi, M Klutz, K Devriendt, et al.
Klinische Monatsblatter Fur Augenheilkunde|March 20, 2013
[Diagnosis and treatment of retinoblastoma: current strategies for effective tumour control and preservation of vision]P Temming, A Eggert, N Bornfeld, et al.
British Journal of Cancer|February 23, 2012
Prognostic significance of chromosome 3 alterations determined by microsatellite analysis in uveal melanoma: a long-term follow-up studyS Thomas, C Pütter, S Weber, et al.
Human Mutation|August 30, 2005
Spectrum of gross deletions and insertions in the RB1 gene in patients with retinoblastoma and association with phenotypic expressionP Albrecht, B Ansperger-Rescher, A Schüler, et al.
American Journal of Human Genetics|August 1, 1997
Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastomaD R Lohmann, M Gerick, B Brandt, et al.
Human Genetics|April 3, 2001
Marked differences in unilateral isolated retinoblastomas from young and older children studied by comparative genomic hybridizationS Herzog, D R Lohmann, K Buiting, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
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.
Journal of Medical Genetics|December 14, 2004
Recurrent deletion of a region containing exon 24 of the RB1 gene caused by non-homologous recombination between a LINE-1HS and MER21B elementP Albrecht, J Bode, K Buiting, et al.
Virchows Archiv. B, Cell Pathology Including Molecular Pathology|January 1, 1993
Identification of p53 gene mutations in gastrointestinal and pancreatic carcinoids by nonradioisotopic SSCAD R Lohmann, A Funk, H P Niedermeyer, et al.
Journal of Medical Genetics|June 1, 1995
Identification of RB1 germline mutations in Argentinian families with sporadic bilateral retinoblastomaI Szijan, D R Lohmann, D L Parma, et al.
European Journal of Human Genetics : EJHG|September 26, 2001
Multiple lipomas linked to an RB1 gene mutation in a large pedigree with low penetrance retinoblastomaM Genuardi, M Klutz, K Devriendt, et al.
Klinische Monatsblatter Fur Augenheilkunde|March 20, 2013
[Diagnosis and treatment of retinoblastoma: current strategies for effective tumour control and preservation of vision]P Temming, A Eggert, N Bornfeld, et al.
British Journal of Cancer|February 23, 2012
Prognostic significance of chromosome 3 alterations determined by microsatellite analysis in uveal melanoma: a long-term follow-up studyS Thomas, C Pütter, S Weber, et al.
Human Mutation|August 30, 2005
Spectrum of gross deletions and insertions in the RB1 gene in patients with retinoblastoma and association with phenotypic expressionP Albrecht, B Ansperger-Rescher, A Schüler, et al.
American Journal of Human Genetics|August 1, 1997
Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastomaD R Lohmann, M Gerick, B Brandt, et al.
Human Genetics|April 3, 2001
Marked differences in unilateral isolated retinoblastomas from young and older children studied by comparative genomic hybridizationS Herzog, D R Lohmann, K Buiting, et al.
Pageof 3