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Seite 1 für „Chromosome“ · Literaturverweise aus öffentlichen Artikeln
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The epidemiology of sex chromosome abnormalities
pubmed · 32506765
Literaturverweis öffnenComplex mosaic form of trisomy chromosome 18 and monosomy chromosome X in a girl with esophageal atresia and mild developmental delay: Diagnostic and therapeutic challenge and a review of literature
pubmed · 42267868
Literaturverweis öffnen[Atypical cat eye syndrome. Fluorescence in situ hybridization of metaphase chromosomes].
pubmed · 1359403
Literaturverweis öffnenIdentification of autosomal and sex chromosome aneuploidies using next generation sequencing
pubmed · 41838401
Literaturverweis öffnen[X chromosome recessively transmitted hydrocephalus with congenital aqueduct stenosis].
pubmed · 3907171
Literaturverweis öffnenPrenatal diagnosis, genetic analysis, and pregnancy outcomes of fetuses with mosaic isodicentric Y chromosomes
pubmed · 42046074
Literaturverweis öffnenSex Chromosome Tetrasomy and Pentasomy
pubmed · 7567329
Literaturverweis öffnenThe Extra X Chromosome and Autoimmune Susceptibility in Klinefelter Syndrome
pubmed · 42400286
Literaturverweis öffnenIdentification of Complex Chromosomal Rearrangement Involving Chromosomes 10, 18, and 19 in a Family Undergoing Prenatal Diagnosis: Case Report
pubmed · 42382047
Literaturverweis öffnenCentromeric instability and chromoanasynthesis observed in nine supernumerary marker chromosomes resolved with long-read genome sequencing
pubmed · 41881544
Literaturverweis öffnenSex chromosome aneuploidies
pubmed · 29325624
Literaturverweis öffnenRates of unbalanced chromosome rearrangements associated with pericentric and paracentric inversions: Analysis of molecular chromosome results in embryo samples
pubmed · 42182041
Literaturverweis öffnenMitotic dynamics of the nuclear lamina in the backstage of chromosome separation
pubmed · 41298957
Literaturverweis öffnenPrenatal diagnosis and clinical evaluation of fetuses with structural X chromosome abnormalities: a ten-year single-center retrospective study
pubmed · 41776513
Literaturverweis öffnenInfluence of X-Chromosome Inactivation in Pathogenesis of Turner Syndrome
pubmed · 42496531
Literaturverweis öffnenAccurate Detection of Multiple Chromosome Rearrangements and Copy Number Variations by PacBio Sequencing in Complex Chromosomal Abnormality
pubmed · 41936057
Literaturverweis öffnenSex chromosome aneuploidies and fertility: 47,XXY, 47,XYY, 47,XXX and 45,X/47,XXX
pubmed · 37399523
Literaturverweis öffnenX-chromosome gene dosage shapes MASLD beyond sex hormones
pubmed · 42191501
Literaturverweis öffnenPrenatal diagnosis of congenital diaphragmatic hernia with mosaicism of chromosomes 17q and 18q in Iran: a case report
pubmed · 42082986
Literaturverweis öffnenCurrent survey of early childhood intervention services in infants and young children with sex chromosome aneuploidies
pubmed · 32449585
Literaturverweis öffnenCase Report: Rare triple-line chromosome 9 mosaicism (47,XX,+del(9)(q13)/47,XX,+9/46,XX) associated with severe neurodevelopmental impairment and congenital anomalies
pubmed · 42017141
Literaturverweis öffnenPrenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result
pubmed · 34247824
Literaturverweis öffnenClinical and Biological Insights into Myelodysplastic Neoplasms Associated with Deletions of Chromosome 5q Region
pubmed · 41440765
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