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Results:
1-12
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Results: 12
Authors:
Fritz, B
Hallermann, C
Olert, J
Fuchs, B
Bruns, M
Aslan, M
Schmidt, S
Coerdt, W
Muntefering, H
Rehder, H
Citation: B. Fritz et al., Cytogenetic analyses of culture failures by comparative genomic hybridisation (CGH) - Re-evaluation of chromosome aberration rates in early spontaneous abortions, EUR J HUM G, 9(7), 2001, pp. 539-547
Authors:
Bartsch, C
Aslan, M
Kohler, J
Miny, P
Horst, J
Holzgreve, W
Rehder, H
Fritz, B
Citation: C. Bartsch et al., Duplication dup(1)(q32q44) detected by comparative genomic hybridization (CGH): Further delineation of trisomies 1q, FETAL DIAGN, 16(5), 2001, pp. 265-273
Authors:
Herzog, S
Lohmann, DR
Buiting, K
Schuler, A
Horsthemke, B
Rehder, H
Rieder, H
Citation: S. Herzog et al., Marked differences in unilateral isolated retinoblastomas from young and older children studied by comparative genomic hybridization, HUM GENET, 108(2), 2001, pp. 98-104
Authors:
Wimmer, K
Eckart, M
Rehder, H
Fonatsch, C
Citation: K. Wimmer et al., Illegitimate splicing of the NF1 gene in healthy individuals mimics mutation-induced splicing alterations in NF1 patients, HUM GENET, 106(3), 2000, pp. 311-313
Authors:
Ramsing, M
Gillessen-Kaesbach, G
Holzgreve, W
Fritz, B
Rehder, H
Citation: M. Ramsing et al., Variability in the phenotypic expression of Fryns syndrome: A report of two sibships, AM J MED G, 95(5), 2000, pp. 415-424
Authors:
Fritz, B
Greber-Platzer, S
Frischer, T
Streubel, B
Groblacher, J
Amann, G
Ventruba, P
Rehder, H
Fonatsch, C
Citation: B. Fritz et al., Familial cryptic translocation with del 4q34 -> qter and dup 12pter -> p13in sibs with tracheal stenosis: C(l)inical, classical and molecular cytogenetic studies and CGH analyses from archival placental tissues evidencing tertiary trisomy 4 in one abortion specimen, AM J MED G, 94(4), 2000, pp. 271-280
Authors:
Aviram-Goldring, A
Fritz, B
Bartsch, C
Steuber, E
Daniely, M
Lev, D
Chaki, R
Barkai, G
Frydman, M
Rehder, H
Citation: A. Aviram-goldring et al., Molecular cytogenetic studies in three patients with partial trisomy 2p, including CGH from paraffin-embedded tissue, AM J MED G, 91(1), 2000, pp. 74-82
Authors:
Fritz, B
Muller-Navia, J
Hillig, U
Kohler, M
Aslan, M
Rehder, H
Citation: B. Fritz et al., Trisomy 2q35-q37 due to insertion of 2q material into 17q25: Clinical, cytogenetic, and molecular cytogenetic characterization, AM J MED G, 87(4), 1999, pp. 297-301
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:
Thies, U
Bartels, I
von Beust, G
Bink, K
Hansmann, I
Rehder, H
Suren, A
Zoll, B
Citation: U. Thies et al., Prenatal diagnosis and fetopathological findings in a fetus with ring chromosome 18, FETAL DIAGN, 13(5), 1998, pp. 315-320
Authors:
Doren, M
Rehder, H
Holzgreve, W
Citation: M. Doren et al., Prenatal diagnosis and obstetric management of Larsen's syndrome in a patient with an unrecognized family history of the disease, GYNECOL OBS, 46(4), 1998, pp. 274-278
Authors:
Fritz, B
Kuster, W
Orstavik, KH
Naumova, A
Spranger, J
Rehder, H
Citation: B. Fritz et al., Pigmentary mosaicism in hypomelanosis of Ito - Further evidence for functional disomy of Xp, HUM GENET, 103(4), 1998, pp. 441-449
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