Chromosome 1p36 Deletion Syndrome: Prenatal Diagnosis, Molecular Cytogenetic Characterization and Fetal Ultrasound Findings

Míreanna Comhchosúla

• Microvillus Inclusion Disease: Prenatal Ultrasound Findings, Molecular Diagnosis and Genetic Counseling of Congenital Diarrhea
  le: Chih-Ping Chen, et al.
  Foilsithe: (2010-12-01)
• Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 20p (20p12-p13) encompassing JAG1 and a literature review of prenatal diagnosis of Alagille syndrome
  le: Chih-Ping Chen, et al.
  Foilsithe: (2017-06-01)
• 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
  le: Chih-Ping Chen, et al.
  Foilsithe: (2010-12-01)
• Prenatal Diagnosis and Molecular Analysis of Trisomy 13 Mosaicism
  le: Chih-Ping Chen, et al.
  Foilsithe: (2009-09-01)
• Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome
  le: Chih-Ping Chen, et al.
  Foilsithe: (2017-12-01)