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Assessment of Potential Communicative Acts in Three Individuals with Rett Syndrome

โœ Scribed by Jeff Sigafoos; Gail Woodyatt; Madonna Tucker; Donna Roberts-Pennell; Nicole Pittendreigh


Book ID
110274246
Publisher
Springer US
Year
2000
Tongue
English
Weight
86 KB
Volume
12
Category
Article
ISSN
1573-3580

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Gross rearrangements in the MECP2 gene i
โœ E. Schollen; E. Smeets; E. Deflem; J.P. Fryns; G. Matthijs ๐Ÿ“‚ Article ๐Ÿ“… 2003 ๐Ÿ› John Wiley and Sons ๐ŸŒ English โš– 162 KB ๐Ÿ‘ 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