Letter: Genetic heterogeneity recognized by Waardenburgh in 1935.

Por Passarge, E
Publicado em 1976

Emil Heitz and the concept of heterochromatin: longitudinal chromosome differentiation was recognized fifty years ago.

Por Passarge, E
Publicado em 1979

Endocardial Fibroelastosis

Por Passarge, E.
Publicado em 1964

Trisomy 8 restricted to cultured fibroblasts.

Por Niss, R, Passarge, E
Publicado em 1976

Microcephalic osteodysplastic primordial dwarfism type I/III in sibs.

Por Meinecke, P, Passarge, E
Publicado em 1991

Somatic mosaicism in a patient with bilateral retinoblastoma.

Por Greger, V, Passarge, E, Horsthemke, B
Publicado em 1990

Alpha1-antitrypsin phenotypes in sex chromosome mosaicism.

Por Kueppers, F, O'Brien, P, Passarge, E, Rüdiger, H W
Publicado em 1975

DNA methylation based testing of 450 patients suspected of having Prader-Willi syndrome.

Por Gillessen-Kaesbach, G, Gross, S, Kaya-Westerloh, S, Passarge, E, Horsthemke, B
Publicado em 1995

A simple and nonradioactive method for detecting the Rb1.20 DNA polymorphism in the retinoblastoma gene.

Por Brandt, B, Greger, V, Yandell, D, Passarge, E, Horsthemke, B
Publicado em 1992

Rate of sister chromatid exchanges in Bloom syndrome fibroblasts reduced by co-cultivation with normal fibroblasts.

Por Rüdiger, H W, Bartram, C R, Harder, W, Passarge, E
Publicado em 1980

Uniparental isodisomy for paternal 2p and maternal 2q in a phenotypically normal female with two isochromosomes, i(2p) and i(2q)

Por ALBRECHT, B., MERGENTHALER, S., EGGERMANN, K., ZERRES, K., PASSARGE, E., EGGERMANN, T.
Publicado em 2001

Application of linkage analysis to genetic counselling in families with hereditary retinoblastoma.

Por Greger, V, Kerst, S, Messmer, E, Höpping, W, Passarge, E, Horsthemke, B
Publicado em 1988

Functional deficiency of fibroblasts heterozygous for Bloom syndrome as specific manifestation of the primary defect.

Por Bartram, C R, Rüdiger, H W, Schmidt-Preuss, U, Passarge, E
Publicado em 1981

Identification of a frameshift mutation in the gene TWIST in a family affected with Robinow-Sorauf syndrome

Por KUNZ, J., HUDLER, M., FRITZ, B., GILLESSEN-KAESBAC..., G., PASSARGE, E.
Publicado em 1999

The spectrum of RB1 germ-line mutations in hereditary retinoblastoma.

Por Lohmann, D. R., Brandt, B., Höpping, W., Passarge, E., Horsthemke, B.
Publicado em 1996

Analysis of a familial three way translocation involving chromosomes 3q, 6q, and 15q by high resolution banding and fluorescent in situ hybridisation (FISH) shows two different unb...

Por Wieczorek, D, Engels, H, Viersbach, R, Henke, B, Schwanitz, G, Passarge, E
Publicado em 1998

Constitutional RB1-gene mutations in patients with isolated unilateral retinoblastoma.

Por Lohmann, D R, Gerick, M, Brandt, B, Oelschläger, U, Lorenz, B, Passarge, E, Horsthemke, B
Publicado em 1997

Bloom's syndrome. VI. The disorder in Israel and an estimation of the gene frequency in the Ashkenazim.

Por German, J, Bloom, D, Passarge, E, Fried, K, Goodman, R M, Katzenellenbogen, I, Laron, Z, Legum, C, Levin, S, Wahrman
Publicado em 1977