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April 2012
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ISSN 1661-8769
EISSN 1661-8777
In this Issue
Molecular Syndromology 2011, Vol. 2, No. 3-5
Title Page / Table of Contents
Mol Syndromol (2012) 2 (3-5): 95–97.
https://doi.org/10.1159/000338223
Paper
Molecular and Clinical Aspects of Angelman Syndrome
Mol Syndromol (2012) 2 (3-5): 100–112.
https://doi.org/10.1159/000328837
CDKL5-Related Disorders: From Clinical Description to Molecular Genetics
Mol Syndromol (2012) 2 (3-5): 137–152.
https://doi.org/10.1159/000331333
FOXG1-Related Disorders: From Clinical Description to Molecular Genetics
Mol Syndromol (2012) 2 (3-5): 153–163.
https://doi.org/10.1159/000327329
The MEF2C-Related and 5q14.3q15 Microdeletion Syndrome
Mol Syndromol (2012) 2 (3-5): 164–170.
https://doi.org/10.1159/000337496
Severe Intellectual Disability Associated with Recessive Defects in CNTNAP2 and NRXN1
Mol Syndromol (2012) 2 (3-5): 181–185.
https://doi.org/10.1159/000331270
The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome)
Mol Syndromol (2012) 2 (3-5): 186–201.
https://doi.org/10.1159/000334260
Update on Kleefstra Syndrome
M.H. Willemsen; A.T. Vulto-van Silfhout; W.M. Nillesen; W.M. Wissink-Lindhout; H. van Bokhoven; N. Philip; E.M. Berry-Kravis; U. Kini; C.M.A. van Ravenswaaij-Arts; B. Delle Chiaie; A.M.M. Innes; G. Houge; T. Kosonen; K. Cremer; M. Fannemel; A. Stray-Pedersen; W. Reardon; J. Ignatius; K. Lachlan; C. Mircher; P.T.J.M. Helderman van den Enden; M. Mastebroek; P.E. Cohn-Hokke; H.G. Yntema; S. Drunat; T. Kleefstra
Mol Syndromol (2012) 2 (3-5): 202–212.
https://doi.org/10.1159/000335648
Adult Phenotypes in Angelman- and Rett-Like Syndromes
Mol Syndromol (2012) 2 (3-5): 217–234.
https://doi.org/10.1159/000335661
Author Index Vol. 2, No. 3–5, 2011
Mol Syndromol (2012) 2 (3-5): 235.
https://doi.org/10.1159/000338224