(Q36772080)

16 August 2017

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title

Chromosomal abnormalities associated with omphalocele (English)

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16 August 2017

Chih-Ping Chen

1

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16 August 2017

publication date

1 March 2007

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Taiwanese Journal of Obstetrics & Gynecology

16 August 2017

published in

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16 August 2017

volume

46

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16 August 2017

issue

1

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16 August 2017

page(s)

1-8

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Omphalocele and gastroschisis: a collaborative study of five Italian congenital malformation registries.

16 August 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Omphalocele and gastroschisis in Europe: a survey of 3 million births 1980-1990. EUROCAT Working Group.

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Correlation between omphalocele contents and karyotypic abnormalities: sonographic study in 37 cases

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Fetal exomphalos and chromosomal defects: relationship to maternal age and gestation

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Characteristics and outcome of 90 cases of fetal omphalocele

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Fetal gastro-intestinal and abdominal wall defects: associated malformations and chromosomal abnormalities

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Fetal exomphalos at 11 to 14 weeks of gestation

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Chromosomal anomalies in newborns with omphalocele

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Fetal omphalocele detected early in pregnancy: associated anomalies and outcomes

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Omphalocele and congenital diaphragmatic hernia associated with fetal trisomy 18

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Ultrasonographic Diagnosis and Perinatal Management of Fetal Abdominal Wall Defects

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Fetal omphalocele: prenatal US detection of concurrent anomalies and other predictors of outcome

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Omphalocele and gastroschisis: an 18-year review study

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

The changing face of gastroschisis and omphalocele in southeast Georgia

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Early prenatal diagnosis of omphalocele constitutes indication for amniocentesis

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Risk factors in congenital abdominal wall defects (omphalocele and gastroschisi): a study in a series of 265,858 consecutive births

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Chromosomal prenatal diagnosis: study of 936 cases of intrauterine abnormalities after ultrasound assessment.

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Omphalocele and gastroschisis in Taiwan

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Prediction of an abnormal karyotype in fetuses with omphalocele

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Prenatal diagnosis and perinatal aspects of abdominal wall defects

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Omphalocele and gastrochisis

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Is there an association of Down Syndrome and omphalocele?

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Turner syndrome associated with an omphalocele

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Monosomy X and omphalocele

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Cystic hygroma and omphalocele at 11 weeks in a fetus with monosomy X

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

X-linked midline defects.

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Chromosomal abnormalities in fetuses with omphalocele. Significance of omphalocele contents

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Prenatal diagnosis of omphalocele associated with umbilical cord cyst.

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Omphalocele and partial trisomy 1q syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Prenatal diagnosis of a fetus with terminal deletion of chromosome 1 (q41)

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

The dup(3q) syndrome: report of eight cases and review of the literature

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Partial duplication of 3q and distal deletion of 11q in a stillbirth with an omphalocele containing the liver, short limbs, and intrauterine growth retardation

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Duplication 3q syndrome: molecular delineation of the critical region

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Further delineation of the dup(3q) syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Recurrent omphalocele with partial trisomy 3q and partial monosomy 11q

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Inconsistency of omphalocoele contents in three consecutive siblings with partial trisomy 3q and partial monosomy 11q

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

De novo partial duplication of 3q and distal deletion of 20p in a 15-week abort us with omphalocele

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Omphalocele in trisomy 3q: further delineation of phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Interstitial deletion 5p accompanied by dicentric ring formation of the deleted segment resulting in trisomy 5p13-cen

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Partial trisomy 6q, due to balanced maternal translocation (6;22) (q21; p13) or (q21; pter)

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Beckwith-Wiedemann syndrome demonstrates a role for epigenetic control of normal development

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Abnormality of chromosome 11 in patients with features of Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Trisomy 11p15 and Beckwith-Wiedemann syndrome. A report of two cases.

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

An infant with Beckwith-Wiedemann syndrome and chromosomal duplication 11p13----pter.: correlation of symptoms between 11p trisomy and Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Paternally inherited duplications of 11p15.5 and Beckwith-Wiedemann syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Recurrent Wiedemann-Beckwith syndrome with inversion of chromosome (11)(p11.2p15.5)

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Molecular analysis of patients with Wiedemann-Beckwith syndrome. II. Paternally derived disomies of chromosome 11

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

NICHD conference. Genomic imprinting: consequences of uniparental disomy for human disease

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Seven cases of Wiedmann-Beckwith syndrome, including the first reported case of mosaic paternal isodisomy along the whole chromosome 11

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Prenatal diagnosis of tetrasomy 47,XY, + i(12p) confirmed byin situ hybridization

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

A further prenatal diagnosis of mosaic tetrasomy 12p (Pallister-Killian syndrome)

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Prenatal ultrasound findings in a fetus with paternal uniparental disomy 14q12-qter

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Paternal UPD14 is responsible for a distinctive malformation complex

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Uniparental disomy (UPD) other than 15: phenotypes and bibliography updated.

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Uniparental isodisomy of chromosome 14 in two cases: an abnormal child and a normal adult

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Paternal uniparental disomy for chromosome 14: a case report and review

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Duplication of distal 15q: report of five new cases from two different translocation kindreds

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Prenatal diagnosis and management of congenital defects of the anterior abdominal wall

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Miller-Dieker syndrome. Detection of a cryptic chromosome translocation using in situ hybridization in a family with multiple affected offspring

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Omphalocele in Miller-Dieker syndrome: expanding the phenotype

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

Brief clinical report: an infant with duplication of 17q21 lead to 17qter.

1 reference

https://api.crossref.org/works/10.1016%2FS1028-4559%2808%2960099-6

7 January 2021

10.1016/S1028-4559(08)60099-6

Identifiers

DOI

1 reference

16 August 2017

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