✦ LIBER ✦

Expression Pattern of the Rett Syndrome Gene MeCP2 in Primate Prefrontal Cortex

✍ Scribed by Schahram Akbarian; Richard Z Chen; Joost Gribnau; Theodore P Rasmussen; Hiu-fai Fong; Rudolf Jaenisch; Edward G Jones

Book ID: 115641644
Publisher: Elsevier Science
Year: 2001
Tongue: English
Weight: 424 KB
Volume: 8
Category: Article
ISSN: 0969-9961
DOI: 10.1006/nbdi.2001.0420

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Mutation analysis of the MECP2 gene in p

Mutation analysis of the MECP2 gene in patients with Rett syndrome

✍ Francesca L. Conforti; Rosalucia Mazzei; Angela Magariello; Alessandra Patitucci 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 46 KB 👁 2 views

The MECP2 Gene Mutation Screening in Ret

The MECP2 Gene Mutation Screening in Rett Syndrome Patients from Croatia

✍ TANJA MATIJEVIĆ; JELENA KNEŽEVIĆ; INGEBORG BARIŠIĆ; BISERKA REŠIĆ; VIDA 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 82 KB

Molecular analysis of MECP2 gene in Egyp

Molecular analysis of MECP2 gene in Egyptian patients with Rett syndrome

✍ Maha S. Zaki; Wessam E. Sharaf El-Din; Germine M. Hamdy; I.H. Kamal; Alice K. Ab 📂 Article 📅 2012 🏛 Springer (Biomed Central Ltd.) 🌐 English ⚖ 764 KB

Gross rearrangements in the MECP2 gene i

Gross rearrangements in the MECP2 gene in three patients with rett syndrome: Implications for routine diagnosis of Rett syndrome

✍ E. Schollen; E. Smeets; E. Deflem; J.P. Fryns; G. Matthijs 📂 Article 📅 2003 🏛 John Wiley and Sons 🌐 English ⚖ 162 KB 👁 1 views

Since 1999, many laboratories have confirmed that mutations in the MECP2 gene are the primary cause of Rett syndrome (RTT or RS) and identified mutations in 70 to 90% of the sporadically affected girls. Most of the screenings are PCR-based and restricted to the coding part of the gene and therefore

Large deletions of the MECP2 gene in Chi

Large deletions of the MECP2 gene in Chinese patients with classical Rett syndrome

✍ H Pan; M-R Li; P Nelson; X-H Bao; X-R Wu; S Yu 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 71 KB

Mutation analysis of the MECP2 gene in B

Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females

✍ Marcella Vacca; Francesco Filippini; Alberta Budillon; Valeria Rossi; Grazia Mer 📂 Article 📅 2000 🏛 Springer 🌐 English ⚖ 214 KB