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Seite 4 für „Chrom“ · Literaturverweise aus öffentlichen Artikeln
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scUnique: 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 öffnenInfluence of X-Chromosome Inactivation in Pathogenesis of Turner Syndrome
pubmed · 42496531
Literaturverweis öffnenLarge asymptomatic pheochromocytoma with incidental metastatic midgut carcinoid tumor
pubmed · 42488370
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 öffnen[Pheochromocytoma in Neurofibromatosis Type 1]
pubmed · 41834598
Literaturverweis öffnenPhäochromozytom und Paragangliom
pubmed · 31338528
Literaturverweis öffnenSex chromosome aneuploidies and fertility: 47,XXY, 47,XYY, 47,XXX and 45,X/47,XXX
pubmed · 37399523
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 öffnenA comprehensive approach for detection of biotin deficiency from dried blood spot samples using liquid chromatography-mass spectrometry
pubmed · 38963009
Literaturverweis öffnenEstablishment of epidemiological cutoff values against Fonsecaea monophora, an agent of chromoblastomycosis and cerebral phaeohyphomycosis
pubmed · 42345564
Literaturverweis öffnenHétérochromie irienne associée à un syndrome de Claude Bernard-Horner acquis
pubmed · 17878817
Literaturverweis öffnenX-chromosome gene dosage shapes MASLD beyond sex hormones
pubmed · 42191501
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 öffnenAssociations between occupational exposure to chromium (VI) and cancers of the oral cavity, small intestine, pancreas, prostate and urinary bladder: systematic review and meta-analyses
pubmed · 42097876
Literaturverweis öffnenA highly rare female phenotype with complex chromosomal mosaicism: 46,XY/45,X/46,X,r(Y)
pubmed · 41285118
Literaturverweis öffnenPrenatal diagnosis of congenital diaphragmatic hernia with mosaicism of chromosomes 17q and 18q in Iran: a case report
pubmed · 42082986
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 öffnenKardiomyopathie bei sekundärer Hämochromatose
doi · 10.1055/s-0042-1744088
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