Prenatal exome sequencing for fetuses with structural abnormalities: the next step-Reference-Cited by-同舟云学术

Prenatal exome sequencing for fetuses with structural abnormalities: the next step

Published:2014-12-09 Issue:1 Volume:45 Page:4-9
ISSN:0960-7692
Container-title:Ultrasound in Obstetrics & Gynecology
language:en
Short-container-title:Ultrasound Obstet Gynecol

Author:

Hillman S.C.¹,Willams D.²,Carss K. J.³,McMullan D.J.⁴,Hurles M. E.³,Kilby M.D.¹

Affiliation:

1. College of Women's and Children's Health & School of Clinical and Experimental Medicine, College of Medicine and DentistryUniversity of Birmingham, Edgbaston, Birmingham, UK; Fetal Medicine Centre, Birmingham Women's Foundation Trust, Edgbaston Birmingham UK

2. Department of Clinical GeneticsBirmingham Women's Foundation Trust Edgbaston Birmingham UK

3. Genome Mutation and Genetic Disease GroupThe Wellcome Trust Sanger Institute, Wellcome Trust Genome Campus Hinxton Cambridge UK

4. West Midlands Genetics LaboratoryBirmingham Women's Foundation Trust Edgbaston Birmingham UK

Publisher

Wiley

Subject

Obstetrics and Gynecology,Radiology, Nuclear Medicine and imaging,Reproductive Medicine,General Medicine,Radiological and Ultrasound Technology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/uog.14653

Reference27 articles.

1. First-trimester ultrasound screening for chromosomal defects

2. The trisomy 18 syndrome

3. Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis

4. Renal Aplasia in Humans Is Associated with RET Mutations

Cited by 59 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. Fetal gene therapy;Journal of Inherited Metabolic Disease;2023-08-07

2. The Impact of Isolated Increased Nuchal Translucency ≥95th Centile on Perinatal Outcome: A Prospective Cohort Study from a North Indian Genetic Center;Journal of Fetal Medicine;2023-04

3. Next-generation sequencing for gene panels, clinical exome, and whole-genome analysis;Human Reproductive and Prenatal Genetics;2023

4. Whole-genome sequencing as a method of prenatal genetic diagnosis: Ethical issues;Clinical Ethics At the Crossroads of Genetic and Reproductive Technologies;2023

5. Application of array comparative genomic hybridization (aCGH) for identification of chromosomal aberrations in the recurrent pregnancy loss;Journal of Assisted Reproduction and Genetics;2022-01-26