Detection of deletions at 7q11.23 in Williams-Beuren syndrome by polymorphic markers-Reference-Cited by-同舟云学术

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Detection of deletions at 7q11.23 in Williams-Beuren syndrome by polymorphic markers

Published:2011 Issue:6 Volume:66 Page:959-964
ISSN:1807-5932
Container-title:Clinics
language:en
Short-container-title:Clinics

Author:

Dutra Roberta Lelis,Pieri Patrícia de Campos,Teixeira Ana Carolina Dias,Honjo Rachel Sayuri,Bertola Debora Romeo,Kim Chong Ae

Publisher

FapUNIFESP (SciELO)

Subject

General Medicine

Link

http://www.scielo.br/pdf/clin/v66n6/07.pdf

Cited by 18 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. Identifying Genetic Etiology in Patients with Intellectual Disability: An Experience in Public Health Services in Northeastern Brazil;Journal of Pediatric Genetics;2022-11-14

2. Sex-specific recombination patterns predict parent of origin for recurrent genomic disorders;BMC Medical Genomics;2021-06-09

3. Spatiotemporal 7q11.23 protein network analysis implicates the role of DNA repair pathway during human brain development;Scientific Reports;2021-04-15

4. Sex-specific recombination predicts parent of origin for recurrent genomic disorders;2020-06-02

5. Growth assessment in children with Williams-Beuren syndrome: a systematic review;Journal of Applied Genetics;2020-03-10

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