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Seite 2 für „chromosomal“ · Literaturverweise aus öffentlichen Artikeln
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Severity-dependent risk of chromosomal abnormalities in fetuses with short long bones: a 10-year cohort study
pubmed · 42108507
Literaturverweis öffnenscUnique: Measuring Ongoing Chromosomal Instability
doi · 10.64898/2026.04.28.721240
Literaturverweis öffnenAccurate Detection of Multiple Chromosome Rearrangements and Copy Number Variations by PacBio Sequencing in Complex Chromosomal Abnormality
pubmed · 41936057
Literaturverweis öffnenCase Report: Optical genome mapping enables identification of complex balanced chromosomal rearrangements
pubmed · 40476266
Literaturverweis öffnenChromosomal abnormalities and pregnancy outcomes in 350 pregnancies with prenatally diagnosed aberrant right subclavian artery: a phenotype-based retrospective cohort study
pubmed · 42219360
Literaturverweis öffnenHybrid Sequencing Characterization of Complex Chromosomal Rearrangements
pubmed · 40884642
Literaturverweis öffnenChromosomal microarray analysis for pregnancies with abnormal maternal serum screening who undergo invasive prenatal testing
pubmed · 34042265
Literaturverweis öffnenThe Anopheles gambiae 2La chromosomal inversion influences chromatin organization and 3D landscape of genes related to malaria transmission
doi · 10.21203/rs.3.rs-9213027/v1
Literaturverweis öffnenChromosomal abnormalities in 478 children with acute myeloid leukemia: clinical characteristics and treatment outcome in a cooperative pediatric oncology group study-POG 8821
pubmed · 10572083
Literaturverweis öffnen11q13.3q13.4 deletion plus 9q21.13q21.33 duplication in an affected girl arising from a familial four-way balanced chromosomal translocation
pubmed · 37475652
Literaturverweis öffnenAntenatal screening for chromosomal abnormalities
pubmed · 35279726
Literaturverweis öffnenA highly rare female phenotype with complex chromosomal mosaicism: 46,XY/45,X/46,X,r(Y)
pubmed · 41285118
Literaturverweis öffnenAcute Myeloid Leukemia, Myelodysplasia-Related (AML-MR), With del(5q) and Double Minutes Containing Chromosomal Segment 11q24 Leading to Amplification and Expression of FLI1
pubmed · 41982344
Literaturverweis öffnenThe role of cytokines in first trimester pregnancy losses with fetal chromosomal anomaly
pubmed · 26817314
Literaturverweis öffnenA case of epilepsy with myoclonic atonic seizures caused by SLC6A1 gene mutation due to balanced chromosomal translocation
pubmed · 36966012
Literaturverweis öffnenFirst prenatal case of jumping-like translocations: unraveling complex chromosomal rearrangements
pubmed · 40069405
Literaturverweis öffnenCost-effectiveness of non-invasive prenatal testing (NIPT) versus direct amniocentesis for screening of fetal chromosomal aneuploidies in Brazilian private health system
pubmed · 41851722
Literaturverweis öffnenIntegrated genomic and clinical indicators for predicting foetal chromosomal abnormalities: development and validation of a nomogram model
pubmed · 41960707
Literaturverweis öffnenPoints to consider for the next-generation-sequencing-based detection of copy-number abnormalities (CNAs) and balanced chromosomal rearrangements in neoplastic disorders: A statement of the American College of Medical Genetics and Genomics (ACMG)
pubmed · 41615347
Literaturverweis öffnenChromosomal Instability Drives Glioblastoma Heterogeneity and Therapeutic Opportunities
pubmed · 42302064
Literaturverweis öffnenMutation profile and chromosomal abnormality in adenomyosis
pubmed · 40679511
Literaturverweis öffnenMeiotic determinants of unbalanced gametogenesis in chromosomal inversion carriers
pubmed · 40957968
Literaturverweis öffnenPreimplantation genetic testing and carrier status detection in patients with balanced chromosomal rearrangements: a real-world multicenter retrospective study
pubmed · 40246052
Literaturverweis öffnenNon-clonal interphase markers of chromosomal instability in malignancy acquisition and cancer progression
pubmed · 42456230
Literaturverweis öffnenImmune reconstitution inflammatory syndrome accompanied by transient immune and chromosomal abnormality after azathioprine exposure in utero
pubmed · 41543248
Literaturverweis öffnenGenetic and functional characterization of inherited complex chromosomal rearrangements in a family with multisystem anomalies
pubmed · 40469905
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