Prenatal Diagnosis of a Female Fetus with Ring Chromosome 9, 46,XX,r(9)(p24q34), and a de novo Interstitial 9p Deletion-Reference-Cited by-同舟云学术

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Prenatal Diagnosis of a Female Fetus with Ring Chromosome 9, 46,XX,r(9)(p24q34), and a de novo Interstitial 9p Deletion

Published:2014 Issue:4 Volume:144 Page:275-279
ISSN:1424-8581
Container-title:Cytogenetic and Genome Research
language:en
Short-container-title:Cytogenet Genome Res

Author:

Penacho Vanessa,Galán Francisco,Martín-Bayón Tina-A.,Mayo Sonia,Manchón Irene,Carrasco Alfonso,Martínez-Castellano Francisco,Alcaraz Luis A.

Publisher

S. Karger AG

Subject

Genetics (clinical),Genetics,Molecular Biology

Cited by 8 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. Ring Chromosome 9;Human Ring Chromosomes;2024

2. MLPA analysis of 32 foetuses with a congenital heart defect and 1 foetus with renal defects - pilot study. The significant frequency rate of presented pathological CNV;Biomedical Papers;2021-03-31

3. Ring chromosome formation by intra‐strand repairing of subtelomeric double stand breaks and clinico‐cytogenomic correlations for ring chromosome 9;American Journal of Medical Genetics Part A;2020-09-26

4. Shone’s complex in a patient with chromosome 9q34.3 deletion (Kleefstra syndrome);Cardiology in the Young;2018-12-26

5. First prenatal diagnosis of a ‘pure’ 9q34.3 deletion (Kleefstra syndrome): A case report and literature review;Journal of Obstetrics and Gynaecology Research;2017-11-21

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