Nordenskjöld M - Search Results

1

Mutations in FLVCR2 associated with Fowler syndrome and survival beyond infancy.

Kvarnung M, Taylan F, Nilsson D, Albåge M, Nordenskjöld M, Anderlid BM, Nordgren A, Syk Lundberg E. Kvarnung M, et al. Among authors: nordenskjold m. Clin Genet. 2016 Jan;89(1):99-103. doi: 10.1111/cge.12565. Epub 2015 Mar 4. Clin Genet. 2016. PMID: 25677735

2

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

3

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

4

Identification of numerical and structural chromosome aberrations in 15 high hyperdiploid childhood acute lymphoblastic leukemias using spectral karyotyping.

Nordgren A, Farnebo F, Johansson B, Holmgren G, Forestier E, Larsson C, Söderhäll S, Nordenskjöld M, Blennow E. Nordgren A, et al. Among authors: nordenskjold m. Eur J Haematol. 2001 May;66(5):297-304. doi: 10.1034/j.1600-0609.2001.066005297.x. Eur J Haematol. 2001. PMID: 11422408

5

Interphase fluorescence in situ hybridization and spectral karyotyping reveals hidden genetic aberrations in children with acute lymphoblastic leukaemia and a normal banded karyotype.

Nordgren A, Schoumans J, Söderhäll S, Nordenskjöld M, Blennow E. Nordgren A, et al. Among authors: nordenskjold m. Br J Haematol. 2001 Sep;114(4):786-93. doi: 10.1046/j.1365-2141.2001.03008.x. Br J Haematol. 2001. PMID: 11564064 Free article.

6

Analysis of short stature homeobox-containing gene ( SHOX) and auxological phenotype in dyschondrosteosis and isolated Madelung deformity.

Grigelioniene G, Schoumans J, Neumeyer L, Ivarsson A, Eklöf O, Enkvist O, Tordai P, Fosdal I, Myhre AG, Westphal O, Nilsson NO, Elfving M, Ellis I, Anderlid BM, Fransson I, Tapia-Paez I, Nordenskjöld M, Hagenäs L, Dumanski JP. Grigelioniene G, et al. Among authors: nordenskjold m. Hum Genet. 2001 Nov;109(5):551-8. doi: 10.1007/s00439-001-0609-y. Epub 2001 Oct 19. Hum Genet. 2001. PMID: 11735031

7

Subtelomeric rearrangements detected in patients with idiopathic mental retardation.

Anderlid BM, Schoumans J, Annerén G, Sahlén S, Kyllerman M, Vujic M, Hagberg B, Blennow E, Nordenskjöld M. Anderlid BM, et al. Among authors: nordenskjold m. Am J Med Genet. 2002 Feb 1;107(4):275-84. doi: 10.1002/ajmg.10029. Am J Med Genet. 2002. PMID: 11840483

8

Detailed characterization of a complex karyotype in a patient with primary plasma cell leukaemia using multicolour spectral karyotyping and micro-FISH.

Nordgren A, Farnebo F, Björkholm M, Sahlén S, Porwit-MacDonald A, Osby E, Kytölä S, Larsson C, Nordenskjöld M, Blennow E. Nordgren A, et al. Among authors: nordenskjold m. Hematol J. 2000;1(2):95-101. doi: 10.1038/sj.thj.6200011. Hematol J. 2000. PMID: 11920176

9

Spectral karyotyping and interphase FISH reveal abnormalities not detected by conventional G-banding. Implications for treatment stratification of childhood acute lymphoblastic leukaemia: detailed analysis of 70 cases.

Nordgren A, Heyman M, Sahlén S, Schoumans J, Söderhäll S, Nordenskjöld M, Blennow E. Nordgren A, et al. Among authors: nordenskjold m. Eur J Haematol. 2002 Jan;68(1):31-41. doi: 10.1034/j.1600-0609.2002.00547.x. Eur J Haematol. 2002. PMID: 11952819

10

FISH-mapping of a 100-kb terminal 22q13 deletion.

Anderlid BM, Schoumans J, Annerén G, Tapia-Paez I, Dumanski J, Blennow E, Nordenskjöld M. Anderlid BM, et al. Among authors: nordenskjold m. Hum Genet. 2002 May;110(5):439-43. doi: 10.1007/s00439-002-0713-7. Epub 2002 Apr 4. Hum Genet. 2002. PMID: 12073014

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