Nordenskjöld M - Search Results

1

Molecular cytogenetic characterization of acute myeloid leukemia and myelodysplastic syndromes with multiple chromosome rearrangements.

Lindvall C, Nordenskjöld M, Porwit A, Björkholm M, Blennow E. Lindvall C, et al. Among authors: nordenskjold m. Haematologica. 2001 Nov;86(11):1158-64. Haematologica. 2001. PMID: 11694401

2

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

3

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

4

Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: prevalence and characterization by fluorescence in situ hybridization.

Blennow E, Bui TH, Kristoffersson U, Vujic M, Annerén G, Holmberg E, Nordenskjöld M. Blennow E, et al. Among authors: nordenskjold m. Prenat Diagn. 1994 Nov;14(11):1019-28. doi: 10.1002/pd.1970141103. Prenat Diagn. 1994. PMID: 7877949

5

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

6

Tetrasomy 15q: two marker chromosomes with no detectable alpha-satellite DNA.

Blennow E, Telenius H, de Vos D, Larsson C, Henriksson P, Johansson O, Carter NP, Nordenskjöld M. Blennow E, et al. Among authors: nordenskjold m. Am J Hum Genet. 1994 May;54(5):877-83. Am J Hum Genet. 1994. PMID: 8178828 Free PMC article.

7

Characterization of supernumerary ring marker chromosomes by fluorescence in situ hybridization (FISH).

Blennow E, Annerén G, Bui TH, Berggren E, Asadi E, Nordenskjöld M. Blennow E, et al. Among authors: nordenskjold m. Am J Hum Genet. 1993 Aug;53(2):433-42. Am J Hum Genet. 1993. PMID: 8328459 Free PMC article.

8

[The gene of spinal muscular atrophy localized. Possibilities for prenatal diagnosis].

Blennow ES, Bui TH, Söderhäll S, Anvret M, Nordenskjöld M. Blennow ES, et al. Among authors: nordenskjold m. Lakartidningen. 1993 Jan 27;90(4):269-75. Lakartidningen. 1993. PMID: 8433608 Swedish. No abstract available.

9

[Preimplantation genetic diagnosis. An alternative to traditional prenatal diagnosis].

Iwarsson E, Blennow ES, Anvret M, Nordenskjöld M, Inzunza J, Ahrlund-Richter L, Pousette A, Hillensjó T, Fridström M, Rosenlund B, Sjöblom P. Iwarsson E, et al. Among authors: nordenskjold m. Lakartidningen. 1997 Aug 27;94(35):2919-22. Lakartidningen. 1997. PMID: 9312603 Review. Swedish. No abstract available.

10

A case of acute lymphoblastic leukemia, near-triploidy, and poor outcome: characterization by fluorescence in situ hybridization using chromosome-specific libraries from all human chromosomes.

Nordgren A, Nordenskjöld M, Söderhäll S, Porwit-MacDonald A, Blennow E. Nordgren A, et al. Among authors: nordenskjold m. Cancer Genet Cytogenet. 1997 Dec;99(2):93-6. doi: 10.1016/s0165-4608(97)00197-0. Cancer Genet Cytogenet. 1997. PMID: 9398861

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