Prenatal Diagnosis of Partial Trisomy 3p (3p21→pter) and Partial Monosomy 11q (11q23→qter) Associated with Abnormal Sonographic Findings of Holoprosencephaly, Orofacial Clefts, Pyelectasis and a Unilateral Duplex Renal System
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference16 articles.
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2. Prenatal diagnosis of de novo distal 11q deletion associated with sonographic findings of unilateral duplex renal system, pyelectasis and orofacial clefts;Chen;Prenat Diagn,2001
3. Prenatal diagnosis of partial trisomy 3p and partial monosomy 11q in a fetus with a Dandy-Walker variant and trigonocephaly;Chen;Prenat Diagn,2002
4. Holoprosencephaly: An Overview and Atlas of Cases;Siebert,1990
5. Multiple hits during early embryonic development: digenic diseases and holoprosencephaly;Ming;Am J Hum Genet,2002
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1. A family study of complex chromosome rearrangement involving chromosomes 1, 8, and 11 and its reproductive consequences;Journal of Assisted Reproduction and Genetics;2017-02-24
2. Case Report 3p partial trisomy and 13q partial monosomy with congenital malformations and psychomotor developmental delay;Genetics and Molecular Research;2013
3. Molecular genetics in fetal neurology;Seminars in Fetal and Neonatal Medicine;2012-12
4. Unbalanced reciprocal translocations at amniocentesis;Taiwanese Journal of Obstetrics and Gynecology;2011-03
5. Partial Trisomy 3p and Partial Monosomy 11q Associated with Atrial Septal Defect, Cleft Palate, and Developmental Delay: A Case Report;Cytogenetic and Genome Research;2011
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