High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation-Reference-Cited by-同舟云学术

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High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation

Published:2008-05-07 Issue:7 Volume:45 Page:447-450
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Jehee F S,Krepischi-Santos A C V,Rocha K M,Cavalcanti D P,Kim C A,Bertola D R,Alonso L G,D'Angelo C S,Mazzeu J F,Froyen G,Lugtenberg D,Vianna-Morgante A M,Rosenberg C,Passos-Bueno M R

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Cited by 35 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. Molecular Mechanisms Involved in Craniosynostosis;In Vivo;2023

2. Comprehensive genetic evaluation of Bulgarian children with syndromic craniosynostosis;Balkan Journal of Medical Genetics;2022-06-01

3. Molecular Genetic Approach to Craniosynostosis Patients and Whole Genome Array CGH Analysis of Nonsyndromic Cases;Gazi Medical Journal;2021-04-01

4. A Pilot Study of Identification Genetic Background of Craniosynostosis Cases;Journal of Craniofacial Surgery;2020-11-25

5. Craniosynostosis: Genetic Basis, Genes, Chromosomes, and Resulting Syndromes;Textbook of Pediatric Neurosurgery;2020

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