Molecular cloning, expression and chromosome location of the human pelota gene PELO
SHAMSADIN, R, ADHAM, I. M, VON BEUST, G, ENGEL, W
Published in Cytogenetic and genome research (01.01.2000)
Published in Cytogenetic and genome research (01.01.2000)
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Journal Article
Assignment of the human melanoma inhibitory activity gene (MIA) to 19q13.32-q13.33 by fluorescence in situ hybridization (FISH)
KOEHLER, M. R, BOSSERHOFF, A.-K, VON BEUST, G, BAUER, A, BLESCH, A, BUETTNER, R, SCHLEGEL, J, BOGDAHN, U, SCHMID, M
Published in Genomics (San Diego, Calif.) (01.07.1996)
Published in Genomics (San Diego, Calif.) (01.07.1996)
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Journal Article
Prenatal Diagnosis and Fetopathological Findings in a Fetus with Ring Chromosome 18
Thies, U., Bartels, I., von Beust, G., Bink, K., Hansmann, I., Rehder, H., Suren, A., Zoll, B.
Published in Fetal diagnosis and therapy (01.09.1998)
Published in Fetal diagnosis and therapy (01.09.1998)
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Journal Article
Assignment of the germ cell cyritestin gene 2 (CYRN2) to human chromosome 16q12.1 by fluorescence in situ hybridization to 5-azacytidine induced, partially decondensed chromosomes
KOEHLER, M. R, VON BEUST, G, ENGEL, W, SCHMID, M
Published in Cytogenetic and genome research (01.01.1997)
Published in Cytogenetic and genome research (01.01.1997)
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Journal Article
DNA analysis of Huntington's disease: five years of experience in Germany, Austria, and Switzerland
Laccone, F, Engel, U, Holinski-Feder, E, Weigell-Weber, M, Marczinek, K, Nolte, D, Morris-Rosendahl, D J, Zühlke, C, Fuchs, K, Weirich-Schwaiger, H, Schlüter, G, von Beust, G, Vieira-Saecker, A M, Weber, B H, Riess, O
Published in Neurology (11.09.1999)
Published in Neurology (11.09.1999)
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Journal Article
Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter → p12.2)[10]
Sauter, S., von Beust, G., Burfeind, P., Weise, A., Starke, H., Liehr, T., Zoll, B.
Published in American journal of medical genetics. Part A (01.08.2003)
Published in American journal of medical genetics. Part A (01.08.2003)
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Journal Article
Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay
von Beust, G., Sauter, S.M., Liehr, T., Burfeind, P., Bartels, I., Starke, H., von Eggeling, F., Zoll, B.
Published in American journal of medical genetics. Part A (15.08.2005)
Published in American journal of medical genetics. Part A (15.08.2005)
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Journal Article
Assignment of the Human Melanoma Inhibitory Activity Gene (MIA) to 19q13.32–q13.33 by Fluorescencein SituHybridization (FISH)
Koehler, M.R., Bosserhoff, A.-K., von Beust, G., Bauer, A., Blesch, A., Buettner, R., Schlegel, J., Bogdahn, U., Schmid, M.
Published in Genomics (San Diego, Calif.) (01.07.1996)
Published in Genomics (San Diego, Calif.) (01.07.1996)
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Journal Article
Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism
Karadima, G, Bugge, M, Nicolaidis, P, Vassilopoulos, D, Avramopoulos, D, Grigoriadou, M, Albrecht, B, Passarge, E, Annerén, G, Blennow, E, Clausen, N, Galla-Voumvouraki, A, Tsezou, A, Kitsiou-Tzeli, S, Hahnemann, J M, Hertz, J M, Houge, G, Kuklík, M, Macek, M, Lacombe, D, Miller, K, Moncla, A, López Pajares, I, Patsalis, P C, Petersen, M B
Published in European journal of human genetics : EJHG (01.09.1998)
Published in European journal of human genetics : EJHG (01.09.1998)
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Journal Article
Molecular cloning, chromosomal localization, and expression analysis of CYRN1 and CYRN2, two human genes coding for cyritestin, a sperm protein involved in gamete interaction
Adham, I M, Kim, Y, Shamsadin, R, Heinlein, U A, Von Beust, G, Mattei, M G, Engel, W
Published in DNA and cell biology (01.02.1998)
Published in DNA and cell biology (01.02.1998)
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Journal Article
Analysis of the Origin of the Extra Chromosome in Trisomy 8 in 4 Cases of Spontaneous Abortions
Nicolaidis, Peter, von Beust, Gabriela, Bugge, Merete, Karadima, Georgia, Vassilopoulos, Dimitris, Brøndum-Nielsen, Karen, Petersen, Michael B.
Published in Fetal diagnosis and therapy (01.01.1998)
Published in Fetal diagnosis and therapy (01.01.1998)
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Journal Article
Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism
Karadima, G, Bugge, M, Nicolaidis, P, Vassilopoulos, D, von Beust, G, Pajares, IL, Albrecht, B, Anneren, G, Avramopoulos, D, Blennow, E, Brondum-Nielsen, K, Clausen, N, Galla-Voumvouraki, A, Grigoriadou, M, Hahnemann, JM, Hertz, JM, Kitsiou-Tzeli, S, Lacombe, D, Miller, K, Moncla, A, Passarge, E, Patsalis, PC, Prieur, M, Tsezou, A, Vekemans, M, Petersen, MB
Published in AMERICAN JOURNAL OF HUMAN GENETICS (1997)
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Published in AMERICAN JOURNAL OF HUMAN GENETICS (1997)
Conference Proceeding
Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay
von Beust, G., Sauter, S.M., Liehr, T., Burfeind, P., Bartels, I., Starke, H., von Eggeling, F., Zoll, B.
Published in American Journal of Medical Genetics Part A (15.08.2005)
Published in American Journal of Medical Genetics Part A (15.08.2005)
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