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Publications by Maj A. Hultén
Disomy 21 in Spermatozoa and the Paternal Origin of Trisomy 21 Down Syndrome
Molecular Cytogenetics
Biochemistry
Molecular Medicine
Genetics
Molecular Biology
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Paternal Uniparental Disomy of Chromosome 21
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Down Syndrome: Characterisation of a Case With Partial Trisomy of Chromosome 21 Owing to a Paternal Balanced Translocation (15;21) (Q26;q22.1) by FISH.
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PCR-Based Detection of Parental Origin of Extra Chromosome 21 in Down Syndrome
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Trisomy 21 and Early Brain Development
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Trisomy 21 and Facial Developmental Instability
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Trisomy 21 Represses Cilia Formation and Function
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Prognostic Impact of Trisomy 21 in Follicular Lymphoma
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A Non-Mosaic Humanized Mouse Model of Down Syndrome, Trisomy of the Long Arm of Human Chromosome 21 in Mouse Chromosome Background