(Q33677591)

English

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

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

0 references

intrauterine growth restriction

1 reference

based on heuristic

inferred from title

author name string

Chen CP

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Liu FF

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Jan SW

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Chen CP

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Lan CC

5

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

language of work or name

0 references

publication date

1 July 1996

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

33

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

615-617

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Prediction of an abnormal karyotype in fetuses with omphalocele

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050675

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050675

14 July 2018

An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050675

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050675

14 July 2018

Ring chromosome 11. A case report and review of the literature.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050675

14 July 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050675

14 July 2018

Distal 11q monosomy. The typical 11q monosomy syndrome is due to deletion of subband 11q24.1

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1050675

30 October 2018

Subchromosomal band interval mapping and ordering of DNA markers in the region 3q26.3-q27 involved in the dup(3q) syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8818953

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Brief clinical report: ring-11 chromosome: phenotype-karyotype correlation with deletions of 11q

1 reference

https://pubmed.ncbi.nlm.nih.gov/8818953

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Early prenatal diagnosis of omphalocele constitutes indication for amniocentesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8818953

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of the long arm of chromosome 11 [46,XX,del(11)(q24.1--qter)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/8818953

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8818953

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fetal omphalocele: associated malformations and chromosomal defects

1 reference

https://pubmed.ncbi.nlm.nih.gov/8818953

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chromosomal abnormalities in fetuses with omphalocele. Significance of omphalocele contents

1 reference

https://pubmed.ncbi.nlm.nih.gov/8818953

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8818953

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Abnormal karyotype of fetuses with omphalocele: prediction based on omphalocele contents

1 reference

https://pubmed.ncbi.nlm.nih.gov/8818953

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Omphalocele and partial trisomy 1q syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/8818953

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.33.7.615

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

0 references

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