Prenatal diagnosis of a fetus with 7q11.23 deletion detected by multiplex ligation-dependent probe amplification (MLPA) screening-Reference-Cited by-同舟云学术

Prenatal diagnosis of a fetus with 7q11.23 deletion detected by multiplex ligation-dependent probe amplification (MLPA) screening

Published:2008 Issue:6 Volume:28 Page:556-558
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Kontos Harry,Manolakos Emmanouil,Malligiannis Pantelis,Plachouras Nicolaos,Ploumis Nikolaos,Mihalatos Markos,Orru Sandro,Anastasiadou Ema,Petersen Michael B.

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference14 articles.

1. Mutational Mechanisms of Williams-Beuren Syndrome Deletions

2. Generation and Comparative Analysis of ∼3.3 Mb of Mouse Genomic Sequence Orthologous to the Region of Human Chromosome 7q11.23 Implicated in Williams Syndrome

3. MLPA as a screening method of aneuploidy and unbalanced chromosomal rearrangements in spontaneous miscarriages

4. Williams syndrome: From genotype through to the cognitive phenotype

5. Cardiovascular manifestations in 75 patients with Williams syndrome

Cited by 12 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. Antenatal ultrasound features of isolated recurrent copy number variation in 7q11.23 (Williams syndrome and 7q11.23 duplication syndrome);Prenatal Diagnosis;2023-03-23

2. Prenatal phenotype features and genetic etiology of the Williams-Beuren syndrome and literature review;Frontiers in Pediatrics;2023-03-17

3. Prenatal Diagnosis of Williams-Beuren Syndrome Based on Suspected Fetal Hypotonia in Early Pregnancy;Cureus;2023-02-10

4. Prenatal diagnosis of Williams-Beuren syndrome by ultrasound and chromosomal microarray analysis;Molecular Cytogenetics;2022-06-28

5. Intrauterine phenotype features of fetuses with Williams–Beuren syndrome and literature review;Annals of Human Genetics;2019-11-11