Hansmann I - Search Results

1

Paternal isodisomy 7q secondary to monosomy 7 at recurrence in a Down syndrome child with acute myelogenous leukemia.

Picos-Cárdenas VJ, Meza-Espinoza JP, Gutiérrez-Angulo M, Esparza-Flores MA, Ayala-Madrigal ML, Hansmann I, González GJ. Picos-Cárdenas VJ, et al. Among authors: hansmann i. Cancer Genet Cytogenet. 2002 Apr 15;134(2):138-41. doi: 10.1016/s0165-4608(01)00607-0. Cancer Genet Cytogenet. 2002. PMID: 12034527

2

Assignment of KPNA4 and KPNB1 encoding karyopherin alpha 4 and beta 1 to human chromosome bands 11q22 and 17q21 respectively, by in situ hybridization.

Ayala-Madrigal ML, Doerr S, Ramírez-Dueñas ML, Hansmann I. Ayala-Madrigal ML, et al. Among authors: hansmann i. Cytogenet Cell Genet. 2000;89(3-4):258-9. doi: 10.1159/000015627. Cytogenet Cell Genet. 2000. PMID: 10965137 No abstract available.

3

Assignment of karyopherin alpha 1 (KPNA1) to human chromosome band 3q21 by in situ hybridization.

Ayala-Madrigal ML, Doerr S, Ramírez-Dueñas ML, Hansmann I. Ayala-Madrigal ML, et al. Among authors: hansmann i. Cytogenet Cell Genet. 2000;90(1-2):58-9. doi: 10.1159/000015661. Cytogenet Cell Genet. 2000. PMID: 11060446 No abstract available.

4

The polymorphic DNA sequence D20S14 is assigned to human chromosome 20p12----p11.2 by in situ hybridization.

Löffler C, Rao VV, Hansmann I. Löffler C, et al. Among authors: hansmann i. Cytogenet Cell Genet. 1992;59(1):20-1. doi: 10.1159/000133190. Cytogenet Cell Genet. 1992. PMID: 1733666

5

Report of the First International Workshop on Human Chromosome 20 Mapping 1993.

Smith CL, Keith T, Hansmann I, Weissenbach J, Asimakopoulos FA, Bowden DW, Deleuze JF, Dutton ER, Fasman KH, Green T, et al. Smith CL, et al. Among authors: hansmann i. Cytogenet Cell Genet. 1994;66(2):78-82. Cytogenet Cell Genet. 1994. PMID: 7904552 No abstract available.

6

Familial mosaicism of del(Y) and inv del(Y).

Röttger S, Pasantes J, Baldermann C, Reichl E, Yen P, Hansmann I, Schempp W. Röttger S, et al. Among authors: hansmann i. Cytogenet Cell Genet. 2000;91(1-4):208-11. doi: 10.1159/000056846. Cytogenet Cell Genet. 2000. PMID: 11173858

7

The human gene for oxytocin-neurophysin I (OXT) is physically mapped to chromosome 20p13 by in situ hybridization.

Rao VV, Löffler C, Battey J, Hansmann I. Rao VV, et al. Among authors: hansmann i. Cytogenet Cell Genet. 1992;61(4):271-3. doi: 10.1159/000133420. Cytogenet Cell Genet. 1992. PMID: 1486803

8

Assignment1 of SUPV3L1 to human chromosome band 10q22.1 by in situ hybridization.

Dmochowska A, Stankiewicz P, Golik P, Stepien PP, Bocian E, Hansmann I, Bartnik E. Dmochowska A, et al. Among authors: hansmann i. Cytogenet Cell Genet. 1998;83(1-2):84-5. doi: 10.1159/000015135. Cytogenet Cell Genet. 1998. PMID: 9925937 No abstract available.

9

The gene for human growth hormone-releasing factor (GHRF) maps to or near chromosome 20p12.

Rao VV, Löffler C, Schnittger S, Hansmann I. Rao VV, et al. Among authors: hansmann i. Cytogenet Cell Genet. 1991;57(1):39-40. doi: 10.1159/000133110. Cytogenet Cell Genet. 1991. PMID: 1855391

10

Kabuki syndrome-like features associated with a small ring chromosome X and XIST gene expression.

Stankiewicz P, Thiele H, Giannakudis I, Schlicker M, Baldermann C, Krüger A, Dörr S, Starke H, Hansmann I. Stankiewicz P, et al. Among authors: hansmann i. Am J Med Genet. 2001 Aug 15;102(3):286-92. doi: 10.1002/ajmg.1462. Am J Med Genet. 2001. PMID: 11484209

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