Could a chimeric condition be responsible for unexpected genetic syndromes? The role of the single nucleotide polymorphism‐array analysis-Reference-Cited by-同舟云学术

Could a chimeric condition be responsible for unexpected genetic syndromes? The role of the single nucleotide polymorphism‐array analysis

Published:2019-01-09 Issue:3 Volume:7 Page:e546
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Bottega Roberta¹^ORCID,Cappellani Stefania¹,Fabretto Antonella¹,Spinelli Alessandro Mauro²,Severini Giovanni Maria¹,Aloisio Michelangelo¹,Faleschini Michela¹,Athanasakis Emmanouil¹,Bruno Irene¹,Faletra Flavio¹,Pecile Vanna¹

Affiliation:

1. Institute for Maternal and Child Health – IRCCS “Burlo Garofolo” Trieste Italy

2. University of Udine Udine Italy

Publisher

Wiley

Subject

Genetics(clinical),Genetics,Molecular Biology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.546

Reference10 articles.

1. A technical application of quantitative next generation sequencing for chimerism evaluation

2. A genomic view of mosaicism and human disease

3. Tetragametic chimerism detected in a healthy woman with mixed-field agglutination reactions in ABO blood grouping

4. Polymorphic Detection of a Parthenogenetic Maternal and Double Paternal Contribution to a 46,XX/46,XY Hermaphrodite

5. Chimaerism shown by cytogenetics and DNA polymorphism analysis.

Cited by 3 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. Case report: Molecular analysis of a 47,XY,+21/46,XX chimera using SNP microarray and review of literature;Frontiers in Genetics;2022-11-11

2. Inheritance of somatic mutations by animal offspring;Science Advances;2022-09-02

3. Prenatal presentation in two fetuses with features of Beckwith Wiedemann syndrome—An unexpected diagnosis of androgenetic chimera and its clinical implications;American Journal of Medical Genetics Part A;2022-02-18