Cornelia de Lange syndrome with ring chromosome 3
- PMID: 2002489
- PMCID: PMC1016788
- DOI: 10.1136/jmg.28.2.143
Cornelia de Lange syndrome with ring chromosome 3
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Cornelia de Lange syndrome with ring chromosome 3.J Med Genet. 1990 Jun;27(6):405-6. doi: 10.1136/jmg.27.6.405. J Med Genet. 1990. PMID: 2359108 Free PMC article. No abstract available.
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Cornelia de Lange syndrome with ring chromosome 3.J Med Genet. 1990 Jun;27(6):405-6. doi: 10.1136/jmg.27.6.405. J Med Genet. 1990. PMID: 2359108 Free PMC article. No abstract available.
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A de novo translocation t(3;17)(q26.3;q23.1) in a child with Cornelia de Lange syndrome.J Med Genet. 1991 Sep;28(9):639-40. doi: 10.1136/jmg.28.9.639. J Med Genet. 1991. PMID: 1956066 Free PMC article.
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Partial trisomy 3q causing mild Cornelia de Lange phenotype.J Med Genet. 1994 Feb;31(2):150-2. doi: 10.1136/jmg.31.2.150. J Med Genet. 1994. PMID: 8182724 Free PMC article.
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[Systemic and ophthalmological findings in Cornelia de Lange syndrome].Klin Oczna. 2012;114(1):68-70. Klin Oczna. 2012. PMID: 22783750 Review. Polish.
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Epileptic features in Cornelia de Lange syndrome: case report and literature review.Brain Dev. 2014 Nov;36(10):837-43. doi: 10.1016/j.braindev.2013.12.008. Epub 2014 Jan 22. Brain Dev. 2014. PMID: 24461912 Review.
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