Jauch A - Search Results

1

Multiplex FISH telomere integrity assay identifies an unbalanced cryptic translocation der(5)t(3;5)(q27;p15.3) in a family with three mentally retarded individuals.

Granzow M, Popp S, Keller M, Holtgreve-Grez H, Brough M, Schoell B, Rauterberg-Ruland I, Hager HD, Tariverdian G, Jauch A. Granzow M, et al. Among authors: jauch a. Hum Genet. 2000 Jul;107(1):51-7. doi: 10.1007/s004390000321. Hum Genet. 2000. PMID: 10982035

2

Study of 30 patients with unexplained developmental delay and dysmorphic features or congenital abnormalities using conventional cytogenetics and multiplex FISH telomere (M-TEL) integrity assay.

Popp S, Schulze B, Granzow M, Keller M, Holtgreve-Grez H, Schoell B, Brough M, Hager HD, Tariverdian G, Brown J, Kearney L, Jauch A. Popp S, et al. Among authors: jauch a. Hum Genet. 2002 Jul;111(1):31-9. doi: 10.1007/s00439-002-0739-x. Epub 2002 Jun 13. Hum Genet. 2002. PMID: 12136233

3

Isochromosome 1q as an early genetic event in a child with intracranial ependymoma characterized by molecular cytogenetics.

Granzow M, Popp S, Weber S, Schoell B, Holtgreve-Grez H, Senf L, Hager D, Boschert J, Scheurlen W, Jauch A. Granzow M, et al. Among authors: jauch a. Cancer Genet Cytogenet. 2001 Oct 1;130(1):79-83. doi: 10.1016/s0165-4608(01)00465-4. Cancer Genet Cytogenet. 2001. PMID: 11672779

4

Multicolor chromosomal bar coding characterizes a de novo interstitial deletion (5)(q33.3q35.2) in a child with multiple congenital malformations.

Schiffer C, Popp S, Moshir S, Rupprath G, Düngfelder E, Hager HD, Tariverdian G, Jauch A. Schiffer C, et al. Among authors: jauch a. Clin Dysmorphol. 2003 Apr;12(2):129-31. doi: 10.1097/00019605-200304000-00011. Clin Dysmorphol. 2003. PMID: 12868477

5

Survival up to age 10 years in a patient with partial duplication 6q: case report and review of the literature.

Seel C, Hager HD, Jauch A, Tariverdian G, Zschocke J. Seel C, et al. Among authors: jauch a. Clin Dysmorphol. 2005 Jan;14(1):51-54. Clin Dysmorphol. 2005. PMID: 15602097

6

High incidence and intraclonal heterogeneity of chromosome 11 aberrations in patients with newly diagnosed multiple myeloma detected by multiprobe interphase FISH.

Cremer FW, Kartal M, Hose D, Bila J, Buck I, Bellos F, Raab MS, Brough M, Moebus A, Hager HD, Goldschmidt H, Moos M, Bartram CR, Jauch A. Cremer FW, et al. Among authors: jauch a. Cancer Genet Cytogenet. 2005 Sep;161(2):116-24. doi: 10.1016/j.cancergencyto.2005.02.015. Cancer Genet Cytogenet. 2005. PMID: 16102581

7

Trisomy 8q and partial trisomy 22 in a 43-year-old man with moderate intellectual disability, epilepsy and large cell non-Hodgkin lymphoma.

Helbig I, Wirtenberger M, Jauch A, Hager HD, Tariverdian G, Hemminki K, Burwinkel B, Klaes R. Helbig I, et al. Among authors: jauch a. Am J Med Genet A. 2006 Aug 1;140(15):1658-62. doi: 10.1002/ajmg.a.31350. Am J Med Genet A. 2006. PMID: 16838305

8

Hodgkin's lymphoma cell lines are characterized by frequent aberrations on chromosomes 2p and 9p including REL and JAK2.

Joos S, Granzow M, Holtgreve-Grez H, Siebert R, Harder L, Martín-Subero JI, Wolf J, Adamowicz M, Barth TF, Lichter P, Jauch A. Joos S, et al. Among authors: jauch a. Int J Cancer. 2003 Feb 10;103(4):489-95. doi: 10.1002/ijc.10845. Int J Cancer. 2003. PMID: 12478664

9

Characterization of two marker chromosomes in a patient with acute nonlymphocytic leukemia by two-color fluorescence in situ hybridization.

Taniwaki M, Speicher MR, Lengauer C, Jauch A, Popp S, Cremer T. Taniwaki M, et al. Among authors: jauch a. Cancer Genet Cytogenet. 1993 Oct 15;70(2):99-102. doi: 10.1016/0165-4608(93)90175-l. Cancer Genet Cytogenet. 1993. PMID: 8242604 Free article.

10

A strategy for the characterization of minute chromosome rearrangements using multiple color fluorescence in situ hybridization with chromosome-specific DNA libraries and YAC clones.

Popp S, Jauch A, Schindler D, Speicher MR, Lengauer C, Donis-Keller H, Riethman HC, Cremer T. Popp S, et al. Among authors: jauch a. Hum Genet. 1993 Dec;92(6):527-32. doi: 10.1007/BF00420933. Hum Genet. 1993. PMID: 8262510

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