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Seite 3 für „Chrom“ · Literaturverweise aus öffentlichen Artikeln
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[Congenital heterochromia of the iris and its explanation].
pubmed · 13080788
Literaturverweis öffnenCase Report: Deciphering a de novo complex chromosomal rearrangement causing premature ovarian insufficiency, short stature, and mild intellectual disability using long-read sequencing
pubmed · 42338980
Literaturverweis öffnenRates of unbalanced chromosome rearrangements associated with pericentric and paracentric inversions: Analysis of molecular chromosome results in embryo samples
pubmed · 42182041
Literaturverweis öffnenCurrent status of functional imaging in neuroblastoma, pheochromocytoma, and paraganglioma disease
pubmed · 30182289
Literaturverweis öffnenSex chromosome aneuploidies
pubmed · 29325624
Literaturverweis öffnenMitotic dynamics of the nuclear lamina in the backstage of chromosome separation
pubmed · 41298957
Literaturverweis öffnenDiagnosis and Management of Pheochromocytoma in Pregnancy: A Multidisciplinary Approach to Treatment and Outcomes at Mbarara Regional Referral Hospital: A Case Report
pubmed · 42445057
Literaturverweis öffnenDiagnostic yield of chromosomal microarray analysis and exome sequencing in fetuses with central nervous system anomalies, with long-term follow-up: a single-center study over a 17-year period
pubmed · 42230359
Literaturverweis öffnenPhäochromozytom im Kindesalter – Contrast-enhanced Ultrasound (CEUS) als mögliche Alternative zur kontrastverstärkten MRT in der Diagnostik von Nebennierentumoren
pubmed · 34077978
Literaturverweis öffnenGenomic and chromosomal Instability: Hidden drivers of Glioblastoma aggressiveness
pubmed · 42425316
Literaturverweis öffnenChromoblastomycosis, Phaeohyphomycotic Abscess, and Sporotrichosis Among American Indian/Alaska Natives, Indian Health Service, 2016-2022
pubmed · 40494319
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 öffnenNormal Fetus in Chromosomal Abnormality Carriers
pubmed · 41078188
Literaturverweis öffnenPredicting Hemodynamic Fluctuations During Adrenalectomy for Pheochromocytoma
pubmed · 41594318
Literaturverweis öffnenChromobox 3 assembles an epigenetic complex contributing to cystathionine γ-lyase-mediated protection against aortic aneurysm/dissection
pubmed · 42236713
Literaturverweis öffnen[X-chromosomal recessive ichthyosis. Detection of heterozygote status in genetically possible carriers by determination of arylsulfatase C activity].
pubmed · 3470217
Literaturverweis öffnenCCRR: a user-friendly platform for analyzing complex chromosomal rearrangements in tumors
pubmed · 40607625
Literaturverweis öffnenThe Extra X Chromosome and Autoimmune Susceptibility in Klinefelter Syndrome
pubmed · 42400286
Literaturverweis öffnenAntenatal screening for chromosomal abnormalities
pubmed · 35279726
Literaturverweis öffnenMitotic microhomology-mediated break-induced replication promotes chromoanasynthesis
pubmed · 41775729
Literaturverweis öffnenPhäochromozytom und Paragangliom
pubmed · 31338528
Literaturverweis öffnenPrenatal diagnosis and clinical evaluation of fetuses with structural X chromosome abnormalities: a ten-year single-center retrospective study
pubmed · 41776513
Literaturverweis öffnenZum Beitrag: Phäochromozytom richtig erkennen, behandeln und nachsorgen
pubmed · 29409093
Literaturverweis öffnenInfluence of X-Chromosome Inactivation in Pathogenesis of Turner Syndrome
pubmed · 42496531
Literaturverweis öffnenSeverity-dependent risk of chromosomal abnormalities in fetuses with short long bones: a 10-year cohort study
pubmed · 42108507
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