HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Partial trisomy 10q (10q25.1 →qter) and partial monosomy 13q (13q34→qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization.

AuthorsChih-Ping Chen, Yi-Ning Su, Fuu-Jen Tsai, Schu-Rern Chern, Chin-Yuan Hsu, Pei-Chen Wu, Chen-Chi Lee, Wen-Lin Chen, Wayseen Wang
JournalTaiwanese journal of obstetrics & gynecology (Taiwan J Obstet Gynecol) Vol. 49 Issue 4 Pg. 539-43 (Dec 2010) ISSN: 1875-6263 [Electronic] China (Republic : 1949- )
PMID21199766 (Publication Type: Case Reports, Letter, Research Support, Non-U.S. Gov't)
Topics
  • Abortion, Induced
  • Adult
  • Amniocentesis
  • Chromosome Deletion
  • Chromosome Disorders
  • Chromosomes, Human, Pair 10
  • Chromosomes, Human, Pair 13
  • Comparative Genomic Hybridization
  • Female
  • Fetal Diseases (diagnostic imaging, genetics)
  • Humans
  • Karyotyping
  • Maternal Age
  • Pregnancy
  • Pyelectasis (diagnostic imaging)
  • Translocation, Genetic
  • Trisomy
  • Ultrasonography, Prenatal

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: