Search Result "22q11.2 deletion syndrome"
Neuroimaging Correlates of 22q11.2 Deletion Syndrome: Implications for Schizophrenia Research
Journal: Current Topics in Medicinal Chemistry
Volume: 12 Issue: 21 Year: 2012 Page: 2303-2313
Author(s): E. Boot,T.A.M.J. van Amelsvoort
Hypoparathyroidism Associated with Benign Thyroid Nodules inDiGeorge-like Syndrome: A Rare Case Report and Literature Review
Journal: Endocrine, Metabolic & Immune Disorders - Drug Targets
Volume: 24 Issue: 7 Year: 2024 Page: 850-856
Author(s): Silvia Martina Ferrari
COMT Implication in Cognitive and Psychiatric Symptoms in Chromosome 22q11 Microdeletion Syndrome: A Selective Review
Journal: CNS & Neurological Disorders - Drug Targets
Volume: 11 Issue: 3 Year: 2012 Page: 273-281
Author(s): Marco Armando,Francesco Papaleo,Stefano Vicari
Mechanistic Approach to Understanding Psychosis Risk in Velocardiofacial Syndrome
Journal: Current Pediatric Reviews
Volume: 5 Issue: 2 Year: 2009 Page: 89-104
Author(s): Vandana Shashi, Margaret N. Berry, Matcheri S. Keshavan
Syndromes with Characteristic Facies
Ebook: Craniofacial Disorders - Orofacial Features and Peculiarities in Dental Treatment
Volume: 1 Year: 2017
Author(s): Marcia Ribeiro Gomide,Gisele da Silva Dalben,Lucimara Teixeira das Neves
Doi: 10.2174/9781681085166117010014
Haploinsufficiency of DNA Damage Response Genes and their Potential Influence in Human Genomic Disorders
Journal: Current Genomics
Volume: 9 Issue: 3 Year: 2008 Page: 137-146
Author(s): Mark ODriscoll
Chromosomal Micro-aberration in a Saudi Family with Juvenile Myoclonic Epilepsy
Journal: CNS & Neurological Disorders - Drug Targets
Volume: 16 Issue: 9 Year: 2017 Page: 1010-1017
Author(s): Muhammad Imran Naseer,Mahmood Rasool,Adeel G. Chaudhary,Sameera Sogaty,Sajjad Karim,Hans-Juergen Schulten,Fehmida Bibi,Peter Natesan Pushparaj,Hussein A. Algahtani,Mohammad H. Al-Qahtani
Controlled Somatic and Germline Copy Number Variation in the Mouse Model
Journal: Current Genomics
Volume: 11 Issue: 6 Year: 2010 Page: 470-480
Author(s): Yann Herault, Arnaud Duchon, Damien Marechal, Matthieu Raveau, Patricia L. Pereira, Emilie Dalloneau, Veronique Brault
Tetralogy of Fallot and Hypoplastic Left Heart Syndrome â Complex Clinical Phenotypes Meet Complex Genetic Networks
Journal: Current Genomics
Volume: 16 Issue: 3 Year: 2015 Page: 141-158
Author(s): Harald Lahm,Patric Schon,Stefanie Doppler,Martina DreÃen,Julie Cleuziou,Marcus-Andre Deutsch,Peter Ewert,Rudiger Lange,Markus Krane
Genes Involved in Hereditary Hearing Impairment
Journal: Current Genomics
Volume: 4 Issue: 5 Year: 2003 Page: 379-415
Author(s): B. Haack, M. Pfister, N. Blin, S. Kupka