Natural history of prenatally diagnosed 46,X,isodicentric Y
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference16 articles.
1. 47,XXY (KLINEFELTER SYNDROME) AND 47,XYY: ESTIMATED RATES OF AND INDICATION FOR POSTNATAL DIAGNOSIS WITH IMPLICATIONS FOR PRENATAL COUNSELLING
2. Prenatal application of fluorescentin situ hybridization (FISH) for identification of a mosaic Y-chromosome marker, IDIC(Yp)
3. The endless quest for sex determination genes
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1. Complex genomic rearrangements of the Y chromosome in a premature infant;Molecular Cytogenetics;2024-08-26
2. Clinical Validation and Diagnostic Utility of Optical Genome Mapping in Prenatal Diagnostic Testing;The Journal of Molecular Diagnostics;2023-04
3. A mosaic karyotype of 45,X/46,X,psu idic(Y)(q12) in a ten-year-old boy: integrating high-throughput sequencing with cytogenetic technique for precise diagnosis and genetic counselling;BMC Pediatrics;2023-03-04
4. Clinical and molecular cytogenetic findings and pregnancy outcomes of fetuses with isochromosome Y;Molecular Cytogenetics;2022-08-04
5. Clinical Validation and Diagnostic Utility of Optical Genome Mapping in Prenatal Diagnostic Testing;2022-05-16
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