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Case Report - Unilateral ureteral triplication with duplex kidney and megaureter, 12/2005
We report a case of duplex kidney with Type-2 ureteral triplication, with one megaureter having stenosis at its lower end and dysplasia of the upper moiety of... 
Duplex kidney, megaureter, ureteral triplication
Journal
Urology, ISSN 0090-4295, 09/2019
Ureteral triplication is a rare congenital anomaly of urinary tract with wide spectrum of presentation. The presentation with incontinence has usually been... 
Journal Article
IEEE Transactions on Electromagnetic Compatibility, ISSN 0018-9375, 8/2019, pp. 1 - 11
Modern electronic systems are performing more and more safety-critical tasks, whereby a robust communication is crucial. To protect those communication... 
hamming | reverberation room simulation | triplication | electromagnetic interference | Communication
Journal Article
by Liu and Old and Miles and Fisher and Weatherall and Clegg
British Journal of Haematology, ISSN 0007-1048, 02/2000, Volume 108, Issue 2, pp. 295 - 299
Journal Article
Nature Communications, ISSN 2041-1723, 05/2014, Volume 5, Issue 1, p. 3930
Journal Article
Geophysical Journal International, ISSN 0956-540X, 2016, Volume 205, Issue 1, pp. 499 - 508
Journal Article
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY, ISSN 1751-5521, 08/2016, Volume 38, Issue 4, pp. 435 - 443
Introduction: Alpha thalassaemia is a highly prevalent disease globally and is a well-known public health problem in Malaysia. The deletional forms of the... 
DIAGNOSIS | detection | HEMOGLOBIN DISORDERS | triplication | ALPHA-THALASSEMIA | alpha thalassaemia | Malaysia | PHENOTYPES | INTERMEDIA | ddPCR | SCREEN | GLOBIN GENE TRIPLICATION | MUTATIONS | HEMATOLOGY
Journal Article
Movement Disorders, ISSN 0885-3185, 03/2018, Volume 33, Issue 3, pp. 402 - 402
Journal Article
Clinical Case Reports, ISSN 2050-0904, 01/2018, Volume 6, Issue 1, pp. 147 - 154
Key Clinical Message 16p11.2 deletions and duplications are commonly associated with autism spectrum disorder and linked to mirrored phenotypes of physical... 
16p11.2 duplication | ASD risk variant | gene triplication | 16p11.2 triplication | 16p11.2 deletion
Journal Article
Parkinsonism and Related Disorders, ISSN 1353-8020, 2015, Volume 21, Issue 8, pp. 981 - 986
Abstract Introduction Triplications of SNCA , the gene encoding for α-synuclein, cause a very rare Mendelian form of early-onset parkinsonism combined with... 
Neurology | Parkinsonism | Triplication | Mutation | Gene | α-synuclein | SNCA | DISEASE | DUPLICATION | alpha-synuclein | LOCUS TRIPLICATION | CLINICAL NEUROLOGY | Pedigree | Humans | Parkinson Disease - diagnosis | Adult | Female | Italy | Male | alpha-Synuclein - genetics | Parkinson Disease - genetics | Parkinson Disease - physiopathology | Siblings | Genetic research | Family | Parkinson's disease | Genes
Journal Article
Blood, ISSN 0006-4971, 10/2018, Volume 132, Issue 15, pp. 1561 - 1567
Intravascular large B-cell lymphoma (IVLBCL) is a rare, clinically aggressive lymphoma entity characterized by an almost exclusive growth of large cells within... 
UNKNOWN ORIGIN | ANTHRACYCLINE-BASED CHEMOTHERAPY | ANGIOTROPIC LYMPHOMA | CLINICAL PRESENTATION | TANDEM TRIPLICATION | BONE-MARROW INVOLVEMENT | LARGE T-CELL | ADHESION MOLECULES | HEMATOLOGY | MALIGNANT ANGIOENDOTHELIOMATOSIS | EXPRESSION
Journal Article
Journal Article
Cytogenetic and Genome Research, ISSN 1424-8581, 2018, Volume 156, Issue 1, pp. 5 - 8
The aim of this study was to investigate the origin of the biallelic trisomic amplification pattern of the X chromosome microsatellite marker DXS1187 in an... 
DIAGNOSIS | Prenatal diagnosis | GENETICS & HEREDITY | Triplication | Xq26.2 | QF-PCR | CELL BIOLOGY
Journal Article