نتائج البحث

Prenatal Diagnosis of Mobile Flap-Like Tissue on the Ventricular Septal Defect in a Newborn with Trisomy 18.

• Authors : Kocabas, Abdullah¹; Akcan, Abdullah Barış²; Kardelen, Fırat¹

• Source: Echocardiography. Oct2011, Vol. 28 Issue 9, pE191-E193. 4p.

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Double Aneuploidy: A Case of Trisomy 21 with XYY.

• Authors : K”ken, Resit¹; Bklmez, Aysegul¹; Nadirgil K”ken, Glengl²

• Source: European Journal of General Medicine. 2011, Vol. 8 Issue 4, p338-341. 4p. 1 Color Photograph, 1 Black and White Photograph.

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Massive-Scale RNA-Seq Analysis of Non Ribosomal Transcriptome in Human Trisomy 21.

• Authors : Costa, Valerio¹; Angelini, Claudia²; D'Apice, Luciana³

• Source: PLoS ONE. 2011, Vol. 6 Issue 4, p1-16. 16p.

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Noninvasive Prenatal Diagnosis of Fetal Trisomy 18 and Trisomy 13 by Maternal Plasma DNA Sequencing.

• Authors : Chen, Eric Z.^1,2; Chiu, Rossa W. K.^1,2; Hao Sun^1,2

• Source: PLoS ONE. 2011, Vol. 6 Issue 7, p1-7. 7p.

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'We've been through it all together': supports for parents with children with rare trisomy conditions.

• Authors : Bruns, D.¹ (AUTHOR); Foerster, K.² (AUTHOR)

• Source: Journal of Intellectual Disability Research. Apr2011, Vol. 55 Issue 4, p361-369. 9p. 2 Charts.

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De novo 7p partial trisomy characterized by subtelomeric FISH and whole-genome array in a girl with mental retardation.

• Source: Molecular Cytogenetics (17558166). 2011, Vol. 4 Issue 1, p21-30. 10p. 2 Color Photographs, 1 Black and White Photograph, 2 Diagrams, 2 Charts.

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Dysregulation of Gene Expression in the Artificial Human Trisomy Cells of Chromosome 8 Associated with Transformed Cell Phenotypes.

• Authors : Nawata, Hisakatsu¹; Kashino, Genro²; Tano, Keizo¹

• Source: PLoS ONE. 2011, Vol. 6 Issue 9, p1-9. 9p.

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Early onset of primary hypogonadism revealed by serum anti-Müllerian hormone determination during infancy and childhood in trisomy 21.

• Authors : Grinspon, R. P.¹; Bedecarrás, P.¹; Ballerini, M. G.¹

• Source: International Journal of Andrology. Oct2011, Vol. 34 Issue 5pt2, pe487-e498. 12p. 3 Charts, 2 Graphs.

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Laterality Preference and Cognition: Cross-Syndrome Comparison of Patients with Trisomy 21 (Down), del7q11.23 (Williams-Beuren) and del22q11.2 (DiGeorge or Velo-Cardio-Facial) Syndromes.

• Authors : Carlier, Michèle¹ ; Desplanches, Aude; Philip, Nicole²

• Source: Behavior Genetics. May2011, Vol. 41 Issue 3, p413-422. 10p. 1 Chart, 1 Graph.

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Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21.

• Authors : Papageorgiou, Elisavet A.¹; Karagrigoriou, Alex²; Tsaliki, Evdokia^1,3,4

• Source: Nature Medicine. Apr2011, Vol. 17 Issue 4, p510-513. 4p. 1 Diagram, 2 Charts, 2 Graphs.

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