We analyzed 61 Angelman syndrome (AS) patients by cytogenetic and molecular techniques. On the basis of molecular findings, the patients were classified into the following 4 groups: familial cases without deletion, familial cases with submicroscopic deletion, sporadic cases with deletion, and sporad
โฆ LIBER โฆ
Molecular and clinical characterization of Angelman syndrome in Chinese patients
โ Scribed by Bai, J.-L.; Qu, Y.-J.; Jin, Y.-W.; Wang, H.; Yang, Y.-L.; Jiang, Y.-W.; Yang, X.-Y.; Zou, L.-P.; Song, F.
- Book ID
- 120251126
- Publisher
- John Wiley and Sons
- Year
- 2013
- Tongue
- English
- Weight
- 566 KB
- Volume
- 85
- Category
- Article
- ISSN
- 0009-9163
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Molecular and clinical study of 61 Angel
โ
Saitoh, Shinji ;Harada, Naoki ;Jinno, Yoshihiro ;Hashimoto, Katsuyo ;Imaizumi, K
๐
Article
๐
1994
๐
John Wiley and Sons
๐
English
โ 632 KB
Molecular and Clinical Aspects of Angelm
โ
Dagli, A.; Buiting, K.; Williams, C.A.
๐
Article
๐
2011
๐
S. Karger AG
๐
English
โ 619 KB
Molecular and clinical overlap of Angelm
โ
Kirkilionis, A. J. ;Chudley, A. E. ;Gregory, C. A. ;Hamerton, J. L.
๐
Article
๐
1991
๐
John Wiley and Sons
๐
English
โ 717 KB
Clinical spectrum and molecular diagnosi
โ
Saitoh, Shinji; Buiting, Karin; Cassidy, Suzanne B.; Conroy, Jeffrey M.; Driscol
๐
Article
๐
1997
๐
John Wiley and Sons
๐
English
โ 305 KB
๐ 2 views
Recent studies have identified a new class of Prader-Willi syndrome (PWS) and Angelman syndrome (AS) patients who have biparental inheritance, but neither the typical deletion nor uniparental disomy (UPD) or translocation. However, these patients have uniparental DNA methylation throughout 15q11-q13
Clinical and EEG patterns in 18 patients
โ
A. Romeo; M. Viri; E.F. Gonano; G. Gobbi; P. Veggiotti; F. Viani
๐
Article
๐
1996
๐
Elsevier Science
๐
English
โ 154 KB
Molecular study of chromosome 15 in 22 p
โ
Joke Beuten; Kathelijne Mangelschots; Inge Buntinx; Paul Coucke; Oebele F. Brouw
๐
Article
๐
1993
๐
Springer
๐
English
โ 729 KB