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7441
Association of MTHFD1 G1958A (rs2236225) gene polymorphism with the risk of congenital heart disease: a systematic review and meta-analysis
Published 2025-01-01“…BMC Medical Genomics…”
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7442
QTL Mapping of Traits Associated with Dual Resistance to the African Stem Borer (Busseola fusca) and Spotted Stem Borer (Chilo partellus) in Sorghum (Sorghum bicolor)
Published 2021-01-01“…International Journal of Genomics…”
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7443
Brain network alterations in anorexia Nervosa: A Multi-Center structural connectivity study
Published 2025-01-01“…NeuroImage: Clinical…”
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7444
A variant W chromosome in Centromochlus heckelii (Siluriformes, Auchenipteridae) and the role of repeated DNA in its heteromorphism
Published 2025-01-01“…Genetics and Molecular Biology…”
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7445
PRETRATAMIENTO EN DOS ETAPAS DEL BAGAZO DE CAÑA PARA LA PRODUCCIÓN DE ETANOL A PARTIR DE XILOSA Y GLUCOSA
Published 2024-10-01“…Revista Centro Azúcar…”
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7446
Genome-Wide Expression Profiles of Hemp (Cannabis sativa L.) in Response to Drought Stress
Published 2018-01-01“…International Journal of Genomics…”
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7447
Characteristic craniofacial defects associated with a novel USP9X truncation mutation
Published 2024-05-01“…Human Genome Variation…”
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7448
Mapping of Novel QTL Regulating Grain Shattering Using Doubled Haploid Population in Rice (Oryza sativa L.)
Published 2016-01-01“…International Journal of Genomics…”
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7449
Hsa_circ_0003220 Drives Chemoresistance of Human NSCLC Cells by Modulating miR-489-3p/IGF1
Published 2023-01-01“…International Journal of Genomics…”
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7450
Monoclonal Gammopathy of Undetermined Significance (MGUS) in a Man with Fragile X-associated Tremor/Ataxia Syndrome
Published 2011-01-01“…Case Reports in Genetics…”
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7451
Identification and Expression Analysis of Sugar Transporter Gene Family in Aspergillus oryzae
Published 2020-01-01“…International Journal of Genomics…”
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7452
Child with Deletion 9p Syndrome Presenting with Craniofacial Dysmorphism, Developmental Delay, and Multiple Congenital Malformations
Published 2013-01-01“…Case Reports in Genetics…”
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7453
Novel frameshift variant of WNT10A in a Japanese patient with hypodontia
Published 2024-01-01“…Human Genome Variation…”
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Article -
7454
Novel Phenotype in Unbalanced 7;9 Translocation with Critical Incidental Finding
Published 2022-01-01“…Case Reports in Genetics…”
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7455
Three Novel Mutations in the NPHS1 Gene in Vietnamese Patients with Congenital Nephrotic Syndrome
Published 2017-01-01“…Case Reports in Genetics…”
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7456
Evidence of Divergent Amino Acid Usage in Comparative Analyses of R5- and X4-Associated HIV-1 Vpr Sequences
Published 2017-01-01“…International Journal of Genomics…”
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7457
Multiple Coronary Artery Microfistulas in a Girl with Kleefstra Syndrome
Published 2016-01-01“…Case Reports in Genetics…”
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7458
ALDH1A3–Linc00284 Axis Mediates the Invasion of Colorectal Cancer by Targeting TGFβ Signaling via Sponging miR-361-5p
Published 2022-01-01“…International Journal of Genomics…”
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7459
MaterniCode: New Bioinformatic Pipeline to Detect Fetal Aneuploidies and Rearrangements Using Next-Generation Sequencing
Published 2024-01-01“…International Journal of Genomics…”
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7460
Post-stroke outcome prediction based on lesion-derived features
Published 2025-01-01“…NeuroImage: Clinical…”
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