Prenatal Diagnosis of Monosomy 17p (17p 13.3 → pter) Associated With Polyhydramnios, Intrauterine Growth Restriction, Ventriculomegaly, and Miller-Dieker Lissencephaly Syndrome in a Fetus

समान संसाधन

• Partial Trisomy 16p (16p12.2→pter) and Partial Monosomy 22q (22q13.31 →qter) Presenting With Fetal Ascites and Ventriculomegaly: Prenatal Diagnosis and Array Comparative Genomic Hybridization Characterization
  द्वारा: Chih-Ping Chen, और अन्य
  प्रकाशित: (2010-12-01)
• Prenatal diagnosis of microdeletion 16p13.11 combination with partial monosomy of 2q37.1-qter and partial trisomy of 7p15.3-pter in a fetus with bilateral ventriculomegaly, agenesis of corpus callosum, and polydactyly
  द्वारा: Pi-Lin Sung, और अन्य
  प्रकाशित: (2012-06-01)
• Maternally Inherited Partial Monosomy 9p (pter → p24.1) and Partial Trisomy 20p (pter → p12.1) Characterized by Microarray Comparative Genomic Hybridization
  द्वारा: Freitas, Érika L., और अन्य
  प्रकाशित: (2011)
• Genomic Organization of the Murine Miller–Dieker/Lissencephaly Region: Conservation of Linkage with the Human Region
  द्वारा: Hirotsune, Shinji, और अन्य
  प्रकाशित: (1997)
• Refinement of a 400-kb Critical Region Allows Genotypic Differentiation between Isolated Lissencephaly, Miller-Dieker Syndrome, and Other Phenotypes Secondary to Deletions of 17p13.3
  द्वारा: Cardoso, Carlos, और अन्य
  प्रकाशित: (2003)