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Publikováno v:
Der Gynakologe. 28(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dc3f75e87ab96ec5b3d79c8ede169839
https://pubmed.ncbi.nlm.nih.gov/7498826
https://pubmed.ncbi.nlm.nih.gov/7498826
Autor:
Holger Hummerich, Susanne C. Szymanski, Elisabeth Schröder, Michael I. Lerman, G. Röhrborn, Farida Latif
Publikováno v:
Human genetics. 92(3)
Von Hippel-Lindau disease is a heritable tumour syndrome caused by the loss of the function of a tumour suppressor gene on the short arm of human chromosome 3. The interval RAF1-D3S18 (3p25–3p26) has been identfied by genetic linkage studies to har
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b12952f077bfa9eeadf269cf4eecc3ad
https://pubmed.ncbi.nlm.nih.gov/8406436
https://pubmed.ncbi.nlm.nih.gov/8406436
Publikováno v:
Human Genetics. 90
Four hundred fifty sperm complements from eight controls were analyzed. A conservative estimate of aneuploidy was 1.8% with a hyperhaploid rate of 0.9% (4/450). The overall frequency of structural aberrations was 8.9% (40/450). The proportion of X-be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac960c5f5ca6c12342a765d3541a9ee7
https://doi.org/10.1007/bf00210762
https://doi.org/10.1007/bf00210762
Publikováno v:
Human genetics. 89(1)
The sperm chromosomes of a man heterozygous for inv(20)(p13q11.2) were analyzed. Twenty-six sperm chromosome complements were examined, of which fourteen contained the normal chromosome, and twelve the inverted chromosome. None of the sperm complemen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9c48ac58b9e21138ccd84b5091161d39
https://pubmed.ncbi.nlm.nih.gov/1577458
https://pubmed.ncbi.nlm.nih.gov/1577458
Autor:
Roger S. Kirby, John D. McConnell, John Fitzpatrick, Claus G. Roehrborn, Michael Wyllie, Peter Boyle
The spectrum of available treatment options for benign prostatic hyperplasia (BPH) is matched by the spectrum of disease severity, and with up to 90% of men in their 80s suffering from BPH to some extent, it is imperative that patients are offered th
Autor:
H. Frohberg, R. Roll, D. Müller, W. Buselmaier, L. Machemer, M. Schulze-Schencking, J. Kratochvilova, R. Lang, G. Röhrborn, U. H. Ehling, J. Dýcka, D. Lorke, H. Wiemann, J. Peh
Publikováno v:
Archives of Toxicology. 39:173-185
The members of the work group “Dominant Lethal Mutations of the ad hoc Committee Chemogenetics” jointly carried out experimental studies in the period from November 1972 until February 1976. On the basis of the results obtained and the experience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd437d3868cc327700e3e1b86a552ba2
https://doi.org/10.1007/bf00368226
https://doi.org/10.1007/bf00368226
Publikováno v:
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 81:117-122
Chromosomal aberration rates in bone-marrow cells and spermatogonia of Chinese hamster were determined after 1.p. injections of cyclophosphamide (13.3, 40 and 120 mg/kg b.w.) and butyl-nitroso urea (30, 60 and 120 mg/kg b.w.). Generally the number of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ac5a8b2a3bcd6145b6ae6dcb58b041b
https://doi.org/10.1016/0027-5107(81)90092-0
https://doi.org/10.1016/0027-5107(81)90092-0
Publikováno v:
Toxicology Letters. 7:143-148
Nine polycyclic aromatic hydrocarbons (PAHs) were investigated by the cell-transformation assay method of Styles. Benzo(a)pyrene [B(a)P], chrysene (CH), 3-methylcholanthrene (3-MC), benz(a)anthracene (BA), benzo(b)fluoranthene [B(b)F], and dibenz(a,h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8dae1579cbed389fbbfe75341a253265
https://doi.org/10.1016/0378-4274(80)90047-8
https://doi.org/10.1016/0378-4274(80)90047-8
Publikováno v:
Human Genetics. 31:59-65
Ein Fall von testicularer Feminisierung wird vorgestellt, der den Karyotyp 47,XXY in allen untersuchten Metaphasen aus Blut- und Hautkulturen hat. Ein solcher Karyotyp legt die Frage nahe, inwieweit sich die Gonosomenkontitution XXY mit dem Syndrom d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f27798efe7a98b3d1d3b46b53526053
https://doi.org/10.1007/bf00270400
https://doi.org/10.1007/bf00270400