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E Passarge

Showing results (71-80 of 151) with videos related to

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Nature Genetics|December 2, 1999
Incorrect use of the term syntenyE Passarge, B Horsthemke, R A Farber
Genetic 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 Passarge
American Journal of Diseases of Children (1960)|August 1, 1970
Association of ectrodactyly, ectodermal dysplasia, and cleft lip-palateR A Rüdiger, W Haase, E Passarge
Lancet (London, England)|December 28, 1974
Letter: Double deletion of X chromosomeT Koske-Westphal, R E Seel, E Passarge
American Journal of Medical Genetics|September 15, 1992
Deletion in one allele and a rare neutral DNA alteration in the other allele of the RB1 gene in a patient with bilateral retinoblastomaB Horsthemke, B Brandt, B Albrecht, et al.
Humangenetik|August 17, 1970
Human chromosomal deficiency: the 4p--syndromeE Passarge, H C Altrogge, R A Rüdiger
Cancer 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 Passarge
Human Genetics|January 1, 1982
Prenatal detection of a fetus hemizygous for the fragile X-chromosomeA Schmidt, E Passarge, E Seemanová, et al.
Human 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 Passarge
Pageof 16

Showing results (71-80 of 151) with videos related to

Sort By:
Pageof 16
Nature Genetics|December 2, 1999
Incorrect use of the term syntenyE Passarge, B Horsthemke, R A Farber
Genetic 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 Passarge
American Journal of Diseases of Children (1960)|August 1, 1970
Association of ectrodactyly, ectodermal dysplasia, and cleft lip-palateR A Rüdiger, W Haase, E Passarge
Lancet (London, England)|December 28, 1974
Letter: Double deletion of X chromosomeT Koske-Westphal, R E Seel, E Passarge
American Journal of Medical Genetics|September 15, 1992
Deletion in one allele and a rare neutral DNA alteration in the other allele of the RB1 gene in a patient with bilateral retinoblastomaB Horsthemke, B Brandt, B Albrecht, et al.
Humangenetik|August 17, 1970
Human chromosomal deficiency: the 4p--syndromeE Passarge, H C Altrogge, R A Rüdiger
Cancer 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 Passarge
Human Genetics|January 1, 1982
Prenatal detection of a fetus hemizygous for the fragile X-chromosomeA Schmidt, E Passarge, E Seemanová, et al.
Human 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 Passarge
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