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American Journal of Human Genetics|June 1, 1990
Somatic mosaicism in a patient with bilateral retinoblastomaV Greger, E Passarge, B HorsthemkeEuropean Journal of Pediatrics|November 1, 1984
Genetic counselling in cystic fibrosis. Results of a survey of 572 familiesE Passarge, B Eckerland, U StephanGenomics|August 1, 1988
Construction of a chromosome 15-specific linking library and identification of potential gene sequencesK Buiting, E Passarge, B HorsthemkeClinical Genetics|April 1, 1979
Bloom's syndrome. VII. Progress report for 1978J German, D Bloom, E PassargeClinical Genetics|September 1, 1977
Bloom's syndrome. V. Surveillance for cancer in affected familiesJ German, D Bloom, E PassargeCytogenetics and Cell Genetics|January 1, 1988
Pachytene analysis in males heterozygous for a familial translocation (9;12;13) (q22; q22; q32) ascertained through a child with partial trisomy 9R Johannisson, U Löhrs, E PassargeBirth Defects Original Article Series|June 1, 1971
Possible genetic heterogeneity of X-linked ichthyosisE Passarge, B Post, E SchöpfDeutsche Medizinische Wochenschrift (1946)|April 1, 1976
[Cytogenetic and clinical findings in suspected Turner's syndrome: results of a five-year study of 207 patients (author's transl)]R Berghoff, R A Rüdiger, E PassargeTeratology|April 1, 1982
Fetal manifestation of a chromosomal disorder: partial duplication of the long arm of chromosome 5 (5q33 to qter)E Passarge, M Bartsch-Sandhoff, H RehderBirth Defects Original Article Series|June 1, 1971
Syndrome of cystic eyelids, palmo-plantar keratosis, hypodontia and hypotrichosis as a possible autosomal recessive traitE Schöpf, H J Schulz, E PassargePageof 31