Prenatal diagnosis and clinical evaluation of fetuses with structural X chromosome abnormalities: a ten-year single-center retrospective study. [PDF]
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Integrating imaging and genomics in prenatal Treacher Collins syndrome: evidence for practice and policy. [PDF]
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Ultrasound and magnetic resonance imaging of fetal gastrointestinal tract disorders. [PDF]
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Human CNTNAP1 Variants Associated With Severe Neurological Deficits: Additional Cases and Literature Review. [PDF]
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Diagnostic 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. [PDF]
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Congenital Pulmonary Airway Malformation Volume Ratio in Fetuses With Congenital Cystic Lung Diseases to Predict Surgery Within 7 Days of Birth. [PDF]
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Challenges in Managing Undiagnosed Prenatal Sacrococcygeal Teratoma-Case Report and Literature Review. [PDF]
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