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Results:
1-11
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Results: 11
Authors:
Lopez-Correa, C
Dorschner, M
Brems, H
Lazaro, C
Clementi, M
Upadhyaya, M
Dooijes, D
Moog, U
Kehrer-Sawatzki, H
Rutkowski, JL
Fryns, JP
Marynen, P
Stephens, K
Legius, E
Citation: C. Lopez-correa et al., Recombination hotspot in NF1 microdeletion patients, HUM MOL GEN, 10(13), 2001, pp. 1387-1392
Authors:
Zechner, U
Wilda, M
Kehrer-Sawatzki, H
Vogel, W
Fundele, R
Hameister, H
Citation: U. Zechner et al., A high density of X-linked genes for general cognitive ability: a run-awayprocess shaping human evolution?, TRENDS GEN, 17(12), 2001, pp. 697-701
Authors:
Jenne, DE
Tinschert, S
Reimann, H
Lasinger, W
Thiel, G
Hameister, H
Kehrer-Sawatzki, H
Citation: De. Jenne et al., Molecular characterization and gene content of breakpoint boundaries in patients with neurofibromatosis type 1 with 17q11.2 microdeletions, AM J HU GEN, 69(3), 2001, pp. 516-527
Authors:
Kehrer-Sawatzki, H
Moschgath, E
Maier, C
Legius, E
Elgar, G
Krone, W
Citation: H. Kehrer-sawatzki et al., Characterization of the Fugu rubripes NLK and FN5 genes flanking the NF1 (neurofibromatosis type 1) gene in the 5 ' direction and mapping of the human counterparts, GENE, 251(1), 2000, pp. 63-71
Authors:
Wilda, M
Bachner, D
Zechner, U
Kehrer-Sawatzki, H
Vogel, W
Hameister, H
Citation: M. Wilda et al., Do the constraints of human speciation cause expression of the same set ofgenes in brain, testis, and placenta?, CYTOG C GEN, 91(1-4), 2000, pp. 300-302
Authors:
Eisenbarth, I
Konig-Greger, D
Wohr, G
Kehrer-Sawatzki, H
Assum, G
Citation: I. Eisenbarth et al., Characterization of an alphoid subfamily located near p-arm sequences on human chromosome 22, CHROMOS RES, 7(1), 1999, pp. 65-69
Authors:
Kehrer-Sawatzki, H
Maier, C
Moschgath, E
Elgar, G
Krone, W
Citation: H. Kehrer-sawatzki et al., Characterization of three genes, AKAP84, BAW and WSB1, located 3 ' to the Neurofibromatosis type 1 locus in Fugu rubripes, GENE, 235(1-2), 1999, pp. 1-11
Authors:
Kehrer-Sawatzki, H
Rock, H
Gotz, H
Siegel, A
Krone, W
Citation: H. Kehrer-sawatzki et al., Monosomy 6 in human cultured fibroblast-like cells permanently stimulated by fibroblast growth factor 1: evidence for selection, CYTOG C GEN, 86(1), 1999, pp. 28-33
Authors:
Streubel, B
Latta, E
Kehrer-Sawatzki, H
Hoffmann, GF
Fonatsch, C
Rehder, H
Citation: B. Streubel et al., Somatic mosaicism of a greater than 1.7-Mb deletion of genomic DNA involving the entire NF1 gene as verified by FISH: Further evidence for a contiguous gene syndrome in 17q11.2, AM J MED G, 87(1), 1999, pp. 12-16
Authors:
Kehrer-Sawatzki, H
Wohr, G
Schempp, W
Eisenbarth, I
Barbi, G
Assum, G
Citation: H. Kehrer-sawatzki et al., Mapping of members of the low-copy-number repetitive DNA sequence family chAB4 within the p arms of human acrocentric chromosomes: characterization of Robertsonian translocations, CHROMOS RES, 6(6), 1998, pp. 429-435
Authors:
Kehrer-Sawatzki, H
Maier, C
Moschgath, E
Elgar, G
Krone, W
Citation: H. Kehrer-sawatzki et al., Genomic characterization of the neurofibromatosis type 1 gene of Fugu rubripes, GENE, 222(1), 1998, pp. 145-153
Risultati:
1-11
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