Nordenskjöld M - Search Results

1

Detailed clinical description of four patients with 1.3 and 2.1 Mb chromosome imbalances derived from a familial t(12;17)(q24.33;q25.3).

Schoumans J, Sanner G, Nordenskjöld M, Anderlid BM. Schoumans J, et al. Among authors: nordenskjold m. Am J Med Genet A. 2005 Apr 30;134(3):254-8. doi: 10.1002/ajmg.a.30611. Am J Med Genet A. 2005. PMID: 15704131

2

Isolation and mapping of polymorphic cosmid clones used for sublocalization of the multiple endocrine neoplasia type 1 (MEN1) locus.

Larsson C, Weber G, Kvanta E, Lewis K, Janson M, Jones C, Glaser T, Evans G, Nordenskjöld M. Larsson C, et al. Among authors: nordenskjold m. Hum Genet. 1992 May;89(2):187-93. doi: 10.1007/BF00217121. Hum Genet. 1992. PMID: 1350263

3

Complete characterization of a large marker chromosome by reverse and forward chromosome painting.

Blennow E, Telenius H, Larsson C, de Vos D, Bajalica S, Ponder BA, Nordenskjöld M. Blennow E, et al. Among authors: nordenskjold m. Hum Genet. 1992 Dec;90(4):371-4. doi: 10.1007/BF00220461. Hum Genet. 1992. PMID: 1483693

4

Identification of twelve new RFLP-markers on chromosome 22q11-qter.

Carlbom E, Sugawa N, Larsson C, Scambler PJ, Dumanski JP, Collins VP, Nordenskjöld M. Carlbom E, et al. Among authors: nordenskjold m. Hum Genet. 1991 Dec;88(2):135-8. doi: 10.1007/BF00206060. Hum Genet. 1991. PMID: 1684561

5

Molecular analysis of 4p deletion associated with Wolf-Hirschhorn syndrome moving the "critical segment" towards the telomere.

Anvret M, Nordenskjöld M, Stolpe L, Johansson L, Bröndum-Nielsen K. Anvret M, et al. Among authors: nordenskjold m. Hum Genet. 1991 Mar;86(5):481-3. doi: 10.1007/BF00194637. Hum Genet. 1991. PMID: 2016087

6

Characterization of add(1)(p36) in non-Hodgkin lymphomas by fluorescence in situ hybridization.

Bajalica S, Brøndum-Nielsen K, Sørensen AG, Pedersen NT, Kristoffersson U, Akerman M, Anderson M, Pisa P, Nordenskjöld M. Bajalica S, et al. Among authors: nordenskjold m. Genes Chromosomes Cancer. 1995 May;13(1):34-9. doi: 10.1002/gcc.2870130106. Genes Chromosomes Cancer. 1995. PMID: 7541641

7

Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization.

Blennow E, Nielsen KB, Telenius H, Carter NP, Kristoffersson U, Holmberg E, Gillberg C, Nordenskjöld M. Blennow E, et al. Among authors: nordenskjold m. Am J Med Genet. 1995 Jan 2;55(1):85-94. doi: 10.1002/ajmg.1320550122. Am J Med Genet. 1995. PMID: 7702104

8

Genetic mapping of a second locus predisposing to hereditary non-polyposis colon cancer.

Lindblom A, Tannergård P, Werelius B, Nordenskjöld M. Lindblom A, et al. Among authors: nordenskjold m. Nat Genet. 1993 Nov;5(3):279-82. doi: 10.1038/ng1193-279. Nat Genet. 1993. PMID: 7903889

9

Identification, characterisation and clinical applications of cosmids from the telomeric and centromeric regions of the long arm of chromosome 22.

Xie YG, Han FY, Bajalica S, Blennow E, Kristoffersson U, Dumanski JP, Nordenskjöld M. Xie YG, et al. Among authors: nordenskjold m. Hum Genet. 1994 Oct;94(4):339-45. doi: 10.1007/BF00201589. Hum Genet. 1994. PMID: 7927325

10

A constitutional mutation within the retinoblastoma gene detected by PFGE.

Janson M, Nordenskjöld M. Janson M, et al. Among authors: nordenskjold m. Clin Genet. 1994 Jan;45(1):5-10. doi: 10.1111/j.1399-0004.1994.tb03981.x. Clin Genet. 1994. PMID: 8149654

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