Cover Image

Prenatal Visualization of Cebocephaly with a Prominent Nose in a Second-trimester Fetus with Alobar Holoprosencephaly and Trisomy 13

Saved in:

Bibliographic Details
Main Authors:	Chih-Ping Chen (Author), Jin-Chung Shih (Author), Chin-Yuan Tzen (Author), Schu-Rern Chern (Author), Chen-Ju Lin (Author), Wayseen Wang (Author)
Format:	Book
Published:	Elsevier, 2008-03-01T00:00:00Z.
Subjects:	article
Online Access:	Connect to this object online.
Tags:	Add Tag No Tags, Be the first to tag this record!

Similar Items

Alobar holoprosencephaly, cebocephaly, and micropenis in a Klinefelter fetus of a diabetic mother
by: Chih-Ping Chen, et al.
Published: (2012)

Alobar holoprosencephaly and Trisomy 13 (Patau syndrome)
by: Andressa Dias Costa, et al.
Published: (2013)

Positive non-invasive prenatal testing for trisomy 13 in the first trimester in a pregnancy with fetal holoprosencephaly, cebocephaly and postaxial polydactyly
by: Chih-Ping Chen
Published: (2024)

Prenatal Diagnosis of Alobar Holoprosencephaly with Cystic Hygroma
by: Tsung-Ying Hsieh, et al.
Published: (2006)

Prenatal diagnosis of alobar holoprosencephaly associated with cyclopia
by: Andreea Cioca, MD, PhD, et al.
Published: (2017)

Prenatal Diagnosis of Alobar Holoprosencephaly, Cyclopia, Proboscis, and Isochromosome 18q in the Second Trimester
by: Meike Bangma, et al.
Published: (2011)

Prenatal Diagnosis and Molecular Analysis of Triploidy in a Fetus With Intrauterine Growth Restriction, Relative Macrocephaly and Holoprosencephaly
by: Chih-Ping Chen, et al.
Published: (2009)

Digynic triploidy in a fetus presenting with semilobar holoprosencephaly
by: Tzu-Yun Chuang, et al.
Published: (2018)

Rapid diagnosis of trisomy 18 of maternal origin by quantitative fluorescent polymerase chain reaction analysis following tissue culture failure for conventional cytogenetic analysis in a fetus with holoprosencephaly, ventricular septal defect, arthrogryposis of bilateral wrists and aplasia of the thumbs
by: Chih-Ping Chen, et al.
Published: (2021)

Antenatally diagnosed alobar holoprosencephaly: A report of two cases
by: C R Srinivasa Babu, et al.
Published: (2017)

Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosum
by: Chih-Ping Chen, et al.
Published: (2020)

Application of quantitative fluorescent polymerase chain reaction analysis for the rapid confirmation of trisomy 13 of maternal origin in a pregnancy with fetal holoprosencephaly, cyclopia, polydactyly, omphalocele and cell culture failure
by: Chih-Ping Chen, et al.
Published: (2022)

First-trimester diagnosis of recurrent omphalocele associated with fetal trisomy 18 but without parental mosaicism
by: Chih-Ping Chen, et al.
Published: (2015)

Rapid diagnosis of trisomy 13 of maternal origin by quantitative fluorescent polymerase chain reaction analysis in a pregnancy with fetal holoprosencephaly, premaxillary agenesis, postaxial polydactyly of left hand and overriding aorta
by: Chih-Ping Chen, et al.
Published: (2021)

Monozygotic twins with trisomy 18 of paternal origin: prenatal diagnosis and molecular cytogenetic characterization in a pregnancy with one structurally abnormal living fetus and one intrauterine fetal demise
by: Chih-Ping Chen, et al.
Published: (2012)

Trisomy 13 Mosaicism Associated With Cyclopia and Cystic Hygroma
by: Chih-Ping Chen, et al.
Published: (2009)

Second-trimester Molecular Prenatal Diagnosis of Sporadic Apert Syndrome Following Sonographic Findings of Mild Ventriculomegaly and Clenched Hands Mimicking Trisomy 18
by: Chih-Ping Chen, et al.
Published: (2010)

Prenatal diagnosis of trisomy 8 mosaicism
by: Chih-Ping Chen, et al.
Published: (2012)

Prenatal Diagnosis and Molecular Analysis of Trisomy 13 Mosaicism
by: Chih-Ping Chen, et al.
Published: (2009)

Concomitant Omphalocele and Anencephaly Associated with Trisomy 18 and Arthrogryposis Diagnosed in Early Pregnancy
by: Chih-Ping Chen, et al.
Published: (2008)

Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetus
by: Chih-Ping Chen, et al.
Published: (2021)

Third-trimester 3D Ultrasound Evaluation of Thanatophoric Dysplasia Type I
by: Chih-Ping Chen, et al.
Published: (2007)

Application of interphase FISH to uncultured amniocytes for rapid confirmation of true trisomy 2 mosaicism in the case of suspected amniocyte mosaicism involving trisomy 2 in a single colony
by: Chih-Ping Chen, et al.
Published: (2013)

Detection of placental mosaic trisomy 17 in a pregnancy associated with mosaicism for trisomy 17 in a single colony at amniocentesis with a favorable outcome
by: Chih-Ping Chen, et al.
Published: (2021)

First-trimester prenatal diagnosis of Ellis-van Creveld syndrome
by: Chih-Ping Chen, et al.
Published: (2012)

Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic double trisomy involving trisomy 7 and trisomy 20 (48,XY,+7,+20) at amniocentesis
by: Chih-Ping Chen, et al.
Published: (2020)

Prenatal Magnetic Resonance Imaging Evaluation of a Digynic Triploid Fetus
by: Chih-Ping Chen, et al.
Published: (2007)

Mosaic trisomy 12 at amniocentesis: Prenatal diagnosis and molecular genetic analysis
by: Chih-Ping Chen, et al.
Published: (2013)

Prenatal diagnosis of mosaic trisomy 9
by: Chih-Ping Chen, et al.
Published: (2011)

Low-level mosaic double trisomy involving trisomy 6 and trisomy 20 (48,XY,+6,+20) at amniocentesis without uniparental disomy (UPD) 6 and UPD 20 in a pregnancy associated with a favorable outcome
by: Chih-Ping Chen, et al.
Published: (2023)

Low-level mosaic trisomy 13 at amniocentesis associated with a favorable outcome in a pregnancy
by: Chih-Ping Chen, et al.
Published: (2020)

Prenatal diagnosis of low-level mosaicism for trisomy 21 by amniocentesis in a pregnancy associated with maternal uniparental disomy of chromosome 21 in the fetus and a favorable outcome
by: Chih-Ping Chen, et al.
Published: (2020)

Low-level mosaic trisomy 13 at amniocentesis in a pregnancy associated with a positive NIPT result suspicious of trisomy 13, a CVS result of mosaic trisomy 13, cytogenetic discrepancy in various tissues and a favorable fetal outcome
by: Chih-Ping Chen, et al.
Published: (2023)

Prenatal Sonographic Features of Fetuses in Trisomy 13 Pregnancies (IV)
by: Chih-Ping Chen
Published: (2010)

Prenatal Sonographic Features of Fetuses in Trisomy 13 Pregnancies (I)
by: Chih-Ping Chen
Published: (2009)

Prenatal Sonographic Features of Fetuses in Trisomy 13 Pregnancies (II)
by: Chih-Ping Chen
Published: (2009)

Prenatal Sonographic Features of Fetuses in Trisomy 13 Pregnancies (III)
by: Chih-Ping Chen
Published: (2009)

First-trimester sonographic demonstration of digynic triploidy
by: Chih-Ping Chen, et al.
Published: (2013)

Prenatal diagnosis of mosaicism for trisomy 11 in a single colony at amniocentesis in a twin pregnancy with a favorable outcome
by: Chih-Ping Chen, et al.
Published: (2021)

Rapid aneuploidy diagnosis of trisomy 18 by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with fetal arachnoid cyst detected in late second trimester
by: Chih-Ping Chen, et al.
Published: (2012)