✦ LIBER ✦

Clinical and molecular characterization of a new syndrome: the case of 3q29 microdeletion syndrome

✍ Scribed by M Koochek

Book ID: 110888159
Publisher: John Wiley and Sons
Year: 2006
Tongue: English
Weight: 198 KB
Volume: 69
Category: Article
ISSN: 0009-9163
DOI: 10.1111/j.1399-0004.2006.00570c.x

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

A novel microdeletion syndrome involving

A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients

✍ Engels, Hartmut; Wohlleber, Eva; Zink, Alexander; Hoyer, Juliane; Ludwig, Kersti 📂 Article 📅 2009 🏛 Nature Publishing Group 🌐 English ⚖ 452 KB

Variable phenotype in 17q12 microdeletio

Variable phenotype in 17q12 microdeletions: Clinical and molecular characterization of a new case

✍ Palumbo, Pietro; Antona, Vincenzo; Palumbo, Orazio; Piccione, Maria; Nardello, R 📂 Article 📅 2014 🏛 Elsevier Science 🌐 English ⚖ 864 KB

Clinical phenotype and molecular charact

Clinical phenotype and molecular characterization of 6q terminal deletion syndrome: Five new cases

✍ Pasquale Striano; Michela Malacarne; Simona Cavani; Mauro Pierluigi; Rosanna Rin 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 178 KB 👁 2 views

Interstitial 9q22.3 microdeletion: clini

Interstitial 9q22.3 microdeletion: clinical and molecular characterisation of a newly recognised overgrowth syndrome

✍ Redon, Richard; Baujat, Geneviève; Sanlaville, Damien; Le Merrer, Martine; Vekem 📂 Article 📅 2006 🏛 Nature Publishing Group 🌐 English ⚖ 370 KB

Autistic and psychiatric findings associ

Autistic and psychiatric findings associated with the 3q29 microdeletion syndrome: Case report and review

✍ Fabiola Quintero-Rivera; Pantea Sharifi-Hannauer; Julian A. Martinez-Agosto 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 358 KB 👁 2 views

## Abstract The screening of individuals with mild dysmorphic features and mental retardation using whole genome scanning technologies has resulted in the delineation of several previously unrecognized microdeletion syndromes. Microdeletion of 3q29 has been recently described as one such new syndro

Clinical and molecular characterization

Clinical and molecular characterization of 17q21.31 microdeletion syndrome in 14 French patients with mental retardation

✍ Christèle Dubourg; Damien Sanlaville; Martine Doco-Fenzy; Cédric Le Caignec; Cha 📂 Article 📅 2011 🏛 Elsevier Science 🌐 English ⚖ 610 KB