Prenatal diagnosis of partial trisomy 10q (10q25.3→qter) and partial monosomy 18q (18q23→qter)
Author:
Publisher
Wiley
Subject
Genetics(clinical),Obstetrics and Gynaecology
Reference12 articles.
1. PRENATAL DIAGNOSIS OF A DELETION OF 18q IN A FETUS ASSOCIATED WITH MULTIPLE-MARKER SCREEN POSITIVE RESULTS
2. Second-trimester sonographic demonstration of retrognathia and bilateral pyelectasis in a fetus with a duplication of chromosome 10q24.1→qter
3. Prenatal diagnosis of de novo mosaic distal 18q deletion associated with congenital anomalies
4. Recurrent fetal pyelectasis in a family with fetuses associated with partial trisomy 10q (10q24.1?qter)
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1. Low-level complex mosaic with multiple cell lines affecting the 18q21.31q21.32 region in a patient with de novo 18q terminal deletion;European Journal of Medical Genetics;2022-11
2. Low-Level Complex Mosaic with Multiple Cell Lines Affecting the 18q21.31q21.32 Region in a Patient with De Novo 18q Terminal Deletion;SSRN Electronic Journal;2022
3. Unbalanced reciprocal translocations at amniocentesis;Taiwanese Journal of Obstetrics and Gynecology;2011-03
4. Blepharophimosis and mental retardation (BMR) phenotypes caused by chromosomal rearrangements: Description in a boy with partial trisomy 10q and monosomy 4q and review of the literature;European Journal of Medical Genetics;2008-03
5. Current World Literature;Current Opinion in Obstetrics & Gynecology;2007-04
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