Publications by authors named "Sigrid Sahlen"

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In vivo differentiated human embryonic stem cells can acquire chromosomal aberrations more frequently than in vitro during the same period.
Marco Zucchelli, Susanne Ström, Frida Holm, Helena Malmgren, Sigrid Sahlén

Stem Cells Dev· December 2012

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Interphase fluorescent in situ hybridization deletion analysis of the 9p21 region and prognosis in childhood acute lymphoblastic leukaemia (ALL): results from a prospective analysis of 519 Nordic patients treated according to the NOPHO-ALL 2000 protocol.
Ekaterina Kuchinskaya, Mats Heyman, Ann Nordgren, Stefan Söderhäll, Erik Forestier

Br J Haematol· March 2011

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Jumping translocation in a phenotypically normal male: A study of mosaicism in spermatozoa, lymphocytes, and fibroblasts.
Erik Iwarsson, Sigrid Sahlén, Ann Nordgren

Am J Med Genet A· August 2009

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Distal 3p deletion syndrome: detailed molecular cytogenetic and clinical characterization of three small distal deletions and review.
Helena Malmgren, Sigrid Sahlén, Katarina Wide, Mikael Lundvall, Elisabeth Blennow

Am J Med Genet A· September 2007

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Subtelomeric rearrangements detected in patients with idiopathic mental retardation.
Britt-Marie Anderlid, Jacqueline Schoumans, Göran Annerén, Sigrid Sahlén, Mårten Kyllerman

Am J Med Genet· February 2002

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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.
Ann Nordgren, Mats Heyman, Sigrid Sahlén, Jacqueline Schoumans, Stefan Söderhäll

Eur J Haematol· January 2002

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