Bibliographic Details
| Title: |
Microdeletion of chromosome 1q21.3 in fraternal twins is associated with mental retardation, microcephaly, and epilepsy. |
| 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 |
