Prenatal diagnosis of a partial trisomy 13q (q14→qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization-Reference-Cited by-同舟云学术

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Prenatal diagnosis of a partial trisomy 13q (q14→qter): phenotype, cytogenetics and molecular characterization by spectral karyotyping and array comparative genomic hybridization

Published:2010 Issue:1 Volume:9 Page:441-448
ISSN:1676-5680
Container-title:Genetics and Molecular Research
language:
Short-container-title:Genet. Mol. Res.

Author:

Machado I.N.,Heinrich J.K.,Campanhol C.,Rodrigues-Peres R.M.,Oliveira F.M.,Barini R.

Publisher

Genetics and Molecular Research

Subject

Genetics,Molecular Biology,General Medicine

Link

http://www.funpecrp.com.br/gmr/year2010/vol9-1/pdf/gmr716.pdf

Cited by 10 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. Moyamoya syndrome secondary to mitochondrial disease in a patient with partial trisomy 13q14 and 13q31: A novel case report and literature review;Heliyon;2023-02

2. Prenatal Sonographic Features of Rare Chromosome 13 Aberrations;The Application of Clinical Genetics;2022-10

3. Identification of partial trisomy 13q in two unrelated patients using single-nucleotide polymorphism array and literature overview;Molecular Cytogenetics;2022-07-28

4. Partial Trisomy 13q/Monosomy 3p Resulting from a Paternal Reciprocal 3p;13q Translocation in a Boy with Facial Dysmorphism and Hypertrophic Cardiomyopathy;Molecular Syndromology;2021

5. Molecular and Cytogenetic Characterization of a Fetus with Mosaic Ring Chromosome 13;Chinese Medical Journal;2017-12-20

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