Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Prenatal diagnosis, ultrasound findings, and pregnancy outcome of 17q12 deletion and duplication syndromes: a retrospective case series.

Archives of gynecology and obstetrics - 1 Dec 2024

Luo Xiaojin, Chen Xiaohang, Cong Xiaoyi, Niu Hongyan, Zhou Fei, Song Jinshuang, Hu Liang, Pei Yuanyuan, Guo Yanyun

Abstract excerpt

OBJECTIVE: Analyze the ultrasound findings, single-nucleotide polymorphism array (SNP-array) results, and pregnancy outcomes of fetuses with 17q12 deletions and duplications in the second and third trimesters. Explore the prenatal ultrasound characteristics and pregnancy outcomes of these fetuses. METHODS: Retrospective data were collected for 16 fetuses diagnosed with 17q12 deletion and seven fetuses with 17q12...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Chromosome Deletion
Share to Chromosome Duplication

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 17

Share to DNA Copy Number Variations

Share to Polymorphism, Single Nucleotide

Share to Pregnancy

Share to Pregnancy Outcome

Share to Ultrasonography, Prenatal

Source

Identifiers

PMID: 39433644
DOI: 10.1007/s00404-024-07789-4

Genes

ACACA
HNF1B
LHX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Prenatal diagnosis, ultrasound findings, and pregnancy outcome of 17q12 deletion and duplication syndromes: a retrospective case series.PMID 39433644Read ↗

Prenatal diagnosis, ultrasound findings and pregnancy outcome of 7q11.23 deletion and duplication syndromes: what are the fetal features?Semantic proximity Read ↗

Prenatal features of 17q12 microdeletion and microduplication syndromes: A retrospective case series.Semantic proximity Read ↗

Prenatal phenotypes and pregnancy outcomes of fetuses with 17p12 microdeletions and microduplications.Semantic proximity Read ↗

Prenatal Genetic Analysis of Fetal 17q12 Microdeletion Syndrome and Relation to Kidney AbnormalitiesSemantic proximity Read ↗

Prenatal diagnosis of 17q12 deletion syndrome: a retrospective case seriesSemantic proximity Read ↗

Prenatal diagnosis of 15q13.3 deletion and duplication syndrome: what do we tell the prospective parents?Semantic proximity Read ↗

Prenatal phenotypes and pregnancy outcomes of fetuses with recurrent 16p13.11 microduplications.Semantic proximity Read ↗

16p13.11 microdeletion/microduplication in fetuses: investigation of associated ultrasound phenotypes, genetic anomalies, and pregnancy outcome follow-upSemantic proximity Read ↗

[Ultrasonographic phenotype and genetic analysis of fetuses with 17q12 microdeletion].Semantic proximity Read ↗

[Prenatal ultrasound and genetic characteristics of 60 fetuses with 16p11.2 microdeletion].Semantic proximity Read ↗

Prenatal diagnosis and family analysis of 17q12 microdeletion syndrome with fetal renal abnormalitiesSemantic proximity Read ↗

Prenatal phenotype of Wolf-Hirschhorn syndrome: A case series and literature review.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.