18q12.3‐q21.1 microdeletion detected in the prenatally alcohol‐exposed dizygotic twin with discordant fetal alcohol syndrome phenotype-Reference-Cited by-同舟云学术

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18q12.3‐q21.1 microdeletion detected in the prenatally alcohol‐exposed dizygotic twin with discordant fetal alcohol syndrome phenotype

Published:2020-02-25 Issue:4 Volume:8 Page:
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Kahila Hanna¹,Marjonen Heidi²,Auvinen Pauliina²,Avela Kristiina³,Riikonen Raili⁴,Kaminen‐Ahola Nina²^ORCID

Affiliation:

1. Department of Obstetrics and Gynecology Helsinki University Hospital and University of Helsinki Helsinki Finland

2. Department of Medical and Clinical Genetics Medicum University of Helsinki Helsinki Finland

3. Department of Clinical Genetics Helsinki University Hospital HUSLAB Helsinki Finland

4. Children's Hospital Kuopio University Hospital University of Eastern Finland Kuopio Finland

Funder

Yrjö Jahnssonin Säätiö

Juho Vainion Säätiö

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1192

Reference34 articles.

1. BiQ Analyzer: visualization and quality control for DNA methylation data from bisulfite sequencing

2. A 5.3Mb deletion in chromosome 18q12.3 as the smallest region of overlap in two patients with expressive speech delay

3. DNA methylation changes at infertility genes in newborn twins conceived by in vitro fertilisation

4. Congenital Anomalies and Anthropometry of 42 Individuals with Deletions of Chromosome 18q

5. Consequences of chromsome18q deletions

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetic Influences on Fetal Alcohol Spectrum Disorder;Genes;2023-01-12

2. Protective and Risk Factors;Fetal Alcohol Spectrum Disorders;2023

3. Immune Signature Variation in Twins With Clinically Different Recurrent Respiratory Papillomatosis;The Laryngoscope;2020-07-28

4. Fetal alcohol spectrum disorders: Genetic and epigenetic mechanisms;Prenatal Diagnosis;2020-05-21

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