1. Les manifestations ophtalmologiques dans le syndrome de délétion du bras long du chromosome 13 : à propos d’un cas
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3. From Genes to Ambiguity: A Case Study Exploring the Enigmatic Connection Between Chromosome 13q Deletion Syndrome and Ambiguous Genitalia
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4. Fetus of 8q22.2q24.3 duplication and 13q33.2q34 deletion derived from a maternal balanced translocation
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5. First report on chromosomal abnormalities in Eastern Morocco: Identification of a new case of a de novo partial trisomy 13q using single-nucleotide polymorphism array
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11. Terminal deletion of chromosome 13 in a fetus with normal NIPT: The added value of invasive prenatal diagnosis in the NIPT era
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12. Prenatal Sonographic Features of Rare Chromosome 13 Aberrations
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13. A rare unbalanced translocation (trisomy 5q33.3‐qter, monosomy 13q34‐qter) results in growth hormone deficiency and brain anomalies
    Alyssa C. M. Joynt et al, 2021, Molecular Genetics & Genomic Medicine CrossRef
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16. Reduced anogenital distance, hematuria and left renal hypoplasia in a patient with 13q33.1–34 deletion: case report and literature review
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17. Deletion of Chromosome 13 due to Different Rearrangements and Impact on Phenotype
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