Microdeletion of chromosome 1q21.3 in fraternal twins is associated with mental retardation, microcephaly, and epilepsy.
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| Title: | Microdeletion of chromosome 1q21.3 in fraternal twins is associated with mental retardation, microcephaly, and epilepsy. |
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| Authors: | Sonmez FM; Developmental Child Neurology Association, Ankara, Turkey., Uctepe E; Department of Medical Genetics, Health Sciences University, Diskapi Yildirim Beyazit Training and Research Hospital, Ankara, Turkey., Aktas D; Damagen Genetic Diagnostic Center, Ankara, Turkey., Alikasifoglu M; Damagen Genetic Diagnostic Center, Ankara, Turkey. |
| Source: | Intractable & rare diseases research [Intractable Rare Dis Res] 2017 Feb; Vol. 6 (1), pp. 61-64. |
| Publication Type: | Case Reports; Journal Article |
| Journal Info: | Publisher: International Advancement Center for Medicine & Health Research Co. (IACMHR Co.) Country of Publication: Japan NLM ID: 101586847 Publication Model: Print Cited Medium: Print ISSN: 2186-3644 (Print) Linking ISSN: 21863644 NLM ISO Abbreviation: Intractable Rare Dis Res Subsets: PubMed not MEDLINE |
| Database: | MEDLINE Ultimate |
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