Prenatal features of 17q12 microdeletion and microduplication syndromes: A retrospective case series
Author:
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology
Reference32 articles.
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3. Confirmation of chromosomal microarray as a first-tier clinical diagnostic test for individuals with developmental delay, intellectual disability, autism spectrum disorders and dysmorphic features;Battaglia;Eur J Paediatr Neurol,2013
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1. Prenatal Genetic Analysis of Fetal 17q12 Microdeletion Syndrome and Relation to Kidney Abnormalities;2023-05-25
2. Genetic autopsy and genetic counseling for a case of fatal oligohydramnios due to de novo 17q12 deletion syndrome;Journal of Obstetrics and Gynaecology Research;2023-03-12
3. Cytogenetic analysis and family research for two cases of chromosome 6 microduplication and chromosome 9 microdeletion: Different clinical manifestations;Gynecology and Obstetrics Clinical Medicine;2023-03
4. Prenatal Genetic Analysis of Kidney Abnormalities;2023-02-24
5. Potter Deformation Sequence Caused by 17q12 Deletion: A Lethal Constellation;Pediatric and Developmental Pathology;2022-12-13
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