Persistent Extreme Surface Solar Radiation and Its Implications on Solar Photovoltaics
Senger, G., Chtirkova, B., Folini, D., Wohland, J., Wild, M.
Published in Earth's future (01.08.2024)
Published in Earth's future (01.08.2024)
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High resolution multicolor-banding : a new technique for refined FISH analysis of human chromosomes
CHUDOBA, I, PLESCH, A, LÖRCH, T, LEMKE, J, CLAUSSEN, U, SENGER, G
Published in Cytogenetic and genome research (01.01.1999)
Published in Cytogenetic and genome research (01.01.1999)
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The homeobox gene MEIS1 is amplified in IMR-32 and highly expressed in other neuroblastoma cell lines
Jones, T.A., Flomen, R.H., Senger, G., Nižetić, D., Sheer, D.
Published in European journal of cancer (1990) (01.12.2000)
Published in European journal of cancer (1990) (01.12.2000)
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Maternal UPD 20 in a hyperactive child with severe growth retardation
Chudoba, I, Franke, Y, Senger, G, Sauerbrei, G, Demuth, S, Beensen, V, Neumann, A, Hansmann, I, Claussen, U
Published in European journal of human genetics : EJHG (01.07.1999)
Published in European journal of human genetics : EJHG (01.07.1999)
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Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review
Heller, Anita, Seidel, J, Hübler, A, Starke, H, Beensen, V, Senger, G, Rocchi, M, Wirth, J, Chudoba, I, Claussen, U, Liehr, T
Published in Journal of medical genetics (01.07.2000)
Published in Journal of medical genetics (01.07.2000)
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Interstitial deletion of chromosome 6q: precise definition of the breakpoints by microdissection, DNA amplification, and reverse painting
Rubtsov, N, Senger, G, Kuzcera, H, Neumann, A, Kelbova, C, Junker, K, Beensen, V, Claussen, U
Published in Human genetics (01.06.1996)
Published in Human genetics (01.06.1996)
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Evidence for a new microdeletion syndrome in 15q21
Liehr, T, Starke, H, Heller, A, Weise, A, Beensen, V, Senger, G, Kittner, G, Prechtel, M, Claussen, U, Seidel, J
Published in International journal of molecular medicine (01.05.2003)
Published in International journal of molecular medicine (01.05.2003)
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Prevalence of celiac disease in first-degree siblings of celiac disease patients
Goel, G K, Pokharna, R K, Khatri, P C, Senger, G S, Joshi, A, Khatri, M, Dalal, A S
Published in Indian journal of gastroenterology (01.01.2007)
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Published in Indian journal of gastroenterology (01.01.2007)
Journal Article
Improved definition of chromosomal breakpoints using high-resolution multicolour banding
LEMKE, Johannes, CHUDOBA, Ilse, SENGER, Gabriele, STUMM, Markus, LONCAREVIC, Ivan F, HENRY, Cathérine, ZABEL, Bernd, CLAUSSEN, Uwe
Published in Human genetics (01.06.2001)
Published in Human genetics (01.06.2001)
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Released chromatin: linearized DNA for high resolution fluorescence in situ hybridization
Senger, G, Jones, T A, Fidlerová, H, Sanséau, P, Trowsdale, J, Duff, M, Sheer, D
Published in Human molecular genetics (01.08.1994)
Published in Human molecular genetics (01.08.1994)
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An SRY-negative 47,XXY mother and daughter
RÖTTGER, S, SCHIEBEL, K, SENGER, G, EBNER, S, SCHEMPP, W, SCHERERA, G
Published in Cytogenetic and genome research (01.01.2000)
Published in Cytogenetic and genome research (01.01.2000)
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Journal Article
PRENATAL DIAGNOSIS OF A HALF-CRYPTIC TRANSLOCATION USING CHROMOSOME MICRODISSECTION
SENGER, G., CHUDOBA, I., FRIEDRICH, U., TOMMERUP, N., CLAUSSEN, U., BRØNDUM-NIELSEN, K.
Published in Prenatal diagnosis (01.04.1997)
Published in Prenatal diagnosis (01.04.1997)
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Journal Article
The origin of human chromosome 2 analyzed by comparative chromosome mapping with a DNA microlibrary
Wienberg, J, Jauch, A, Lüdecke, H J, Senger, G, Horsthemke, B, Claussen, U, Cremer, T, Arnold, N, Lengauer, C
Published in Chromosome research (01.09.1994)
Published in Chromosome research (01.09.1994)
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