Kalscheuer V - Search Results

1

Familial MCA/MR syndrome due to inherited submicroscopic translocation t(18;21)(q22.1q21.3) with breakpoint at the Down syndrome critical region.

Horn D, Neitzel H, Tönnies H, Kalscheuer V, Kunze J, Hinkel GK, Bartsch O. Horn D, et al. Among authors: kalscheuer v. Am J Med Genet A. 2003 Mar 15;117A(3):236-44. doi: 10.1002/ajmg.a.10017. Am J Med Genet A. 2003. PMID: 12599186 Review.

2

Transcriptional activity of constitutive heterochromatin in the mammal Microtus agrestis (Rodentia, Cricetidae).

Sperling K, Kalscheuer V, Neitzel H. Sperling K, et al. Among authors: kalscheuer v. Exp Cell Res. 1987 Dec;173(2):463-72. doi: 10.1016/0014-4827(87)90286-2. Exp Cell Res. 1987. PMID: 2446895

3

Evolution of the gonosomal heterochromatin of Microtus agrestis: rapid amplification of a large, multimeric, repeat unit containing a 3.0-kb (GATA)11-positive, middle repetitive element.

Kalscheuer V, Singh AP, Nanda I, Sperling K, Neitzel H. Kalscheuer V, et al. Cytogenet Cell Genet. 1996;73(3):171-8. doi: 10.1159/000134333. Cytogenet Cell Genet. 1996. PMID: 8697802

4

Beta-heterochromatin in mammals: evidence from studies in Microtus agrestis based on the extensive accumulation of L1 and non-L1 retroposons in the heterochromatin.

Neitzel H, Kalscheuer V, Henschel S, Digweed M, Sperling K. Neitzel H, et al. Among authors: kalscheuer v. Cytogenet Cell Genet. 1998;80(1-4):165-72. doi: 10.1159/000014974. Cytogenet Cell Genet. 1998. PMID: 9678352

5

Differences in the meiotic pairing behavior of gonosomal heterochromatin between female and male Microtus agrestis: implications for the mechanism of heterochromatin amplification on the X and Y.

Singh A, Henschel S, Sperling K, Kalscheuer V, Neitzel H. Singh A, et al. Among authors: kalscheuer v. Cytogenet Cell Genet. 2000;91(1-4):253-60. doi: 10.1159/000056854. Cytogenet Cell Genet. 2000. PMID: 11173866

6

Comparative genomic hybridization based strategy for the analysis of different chromosome imbalances detected in conventional cytogenetic diagnostics.

Tönnies H, Stumm M, Wegner RD, Chudoba I, Kalscheuer V, Neitzel H. Tönnies H, et al. Among authors: kalscheuer v. Cytogenet Cell Genet. 2001;93(3-4):188-94. doi: 10.1159/000056983. Cytogenet Cell Genet. 2001. PMID: 11528111

7

A cryptic deletion of 2q35 including part of the PAX3 gene detected by breakpoint mapping in a child with autism and a de novo 2;8 translocation.

Borg I, Squire M, Menzel C, Stout K, Morgan D, Willatt L, O'Brien PC, Ferguson-Smith MA, Ropers HH, Tommerup N, Kalscheuer VM, Sargan DR. Borg I, et al. Among authors: kalscheuer vm. J Med Genet. 2002 Jun;39(6):391-9. doi: 10.1136/jmg.39.6.391. J Med Genet. 2002. PMID: 12070244 Free PMC article.

8

Copy and paste: the impact of a new non-L1 retroposon on the gonosomal heterochromatin of Microtus agrestis.

Neitzel H, Kalscheuer V, Singh AP, Henschel S, Sperling K. Neitzel H, et al. Among authors: kalscheuer v. Cytogenet Genome Res. 2002;96(1-4):179-85. doi: 10.1159/000063036. Cytogenet Genome Res. 2002. PMID: 12438796

9

Spectrum of mutations in PTPN11 and genotype-phenotype correlation in 96 patients with Noonan syndrome and five patients with cardio-facio-cutaneous syndrome.

Musante L, Kehl HG, Majewski F, Meinecke P, Schweiger S, Gillessen-Kaesbach G, Wieczorek D, Hinkel GK, Tinschert S, Hoeltzenbein M, Ropers HH, Kalscheuer VM. Musante L, et al. Eur J Hum Genet. 2003 Feb;11(2):201-6. doi: 10.1038/sj.ejhg.5200935. Eur J Hum Genet. 2003. PMID: 12634870

10

High rate of constitutional chromosomal rearrangements in apparently sporadic ALS.

Meyer T, Alber B, Roemer K, Martin T, Kalscheuer VM, Göttert E, Zang KD, Ludolph AC, Ropers HH, Prudlo J. Meyer T, et al. Among authors: kalscheuer vm. Neurology. 2003 Apr 22;60(8):1348-50. doi: 10.1212/01.wnl.0000055088.52681.f1. Neurology. 2003. PMID: 12707441

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