Could acrocallosal syndrome and Greig syndrome affect the same developmental gene?
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference5 articles.
1. Acrocallosal syndrome: Additional manifestations;Casamassima;Am J Med Genet,1989
2. Acrocallosal syndrome: New findings;Moeschler;Am J Med Genet,1989
3. A craniosynostosis in a boy with a del(7)(p15, 3p21.3): Assignment by deletion mapping of the critical segment for craniosynostosis to the mid-portion of 7p21;Motegi;Hum Genet,1985
4. Acrocallosal syndrome in a girl born to consanguineous parents;Salgado;Am J Med Genet,1989
5. Hypogenitalism in the acrocallosal syndrome;Temtamy;Am J Med Genet,1989
Cited by 6 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. A de novoGLI3mutation in a patient with acrocallosal syndrome;American Journal of Medical Genetics Part A;2013-04-30
2. Acrocallosal syndrome in Algerian boy born to consanguineous parents: Review of the literature and further delineation of the syndrome;American Journal of Medical Genetics;1997-03-03
3. Acrocallosal Syndrome: Association with Cystic Malformation of the Brain and Neurodevelopmental Aspects;Neuropediatrics;1992-12
4. The acrocallosal syndrome and Greig syndrome are not allelic disorders.;Journal of Medical Genetics;1992-09-01
5. Absence of the Corpus Callosum;Genetically Defined Animal Models of Neurobehavioral Dysfunctions;1992
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