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Results 1 to 25 of 131

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Failure to Confirm Association Between PIK4CA and Psychosis in 22q11.2 Deletion SyndromeIKEDA, Masashi; WILLIAMS, Nigel; WILLIAMS, Hywel J et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2010, Vol 153, Num 4, pp 980-982, issn 1552-4841, 3 p.Article

Practical Guidelines for Managing Patients with 22q11.2 Deletion SyndromeBASSETT, Anne S; MCDONALD-MCGINN, Donna M; SWILLEN, Ann et al.The Journal of pediatrics. 2011, Vol 159, Num 2, pp 332-339, issn 0022-3476, 8 p.Article

Speech and Hearing in Adults with 22q11.2 Deletion SyndromePERSSON, Christina; FRIMAN, Vanda; OSKARSDOTTIR, Solveig et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 12, pp 3071-3079, issn 1552-4825, 9 p.Article

Hypoparathyroidism and autoimmunity in the 22q11.2 deletion syndromeLIMA, Kari; ABRAHAMSEN, Tore G; BOE WOLFF, Anette et al.European journal of endocrinology. 2011, Vol 165, Num 2, pp 345-352, issn 0804-4643, 8 p.Article

Outcome of Velopharyngoplasty in Patients With Velocardiofacial SyndromeWIDDERSHOVEN, Josine C. C; STUBENITSKY, Bart M; BREUGEM, Corstiaan C et al.Archives of otolaryngology, head & neck surgery. 2008, Vol 134, Num 11, pp 1159-1164, issn 0886-4470, 6 p.Article

Premorbid adjustment and schizophrenia in individuals with 22q11.2 deletion syndromeYUEN, Tracy; CHOW, Eva W. C; SILVERSIDES, Candice K et al.Schizophrenia research. 2013, Vol 151, Num 1-3, pp 221-225, issn 0920-9964, 5 p.Article

La microdélétion 22qII.2 = 22q II.2 microdeletionSCHNEIDER, M; ELIEZ, S.Archives de pédiatrie (Paris). 2010, Vol 17, Num 4, pp 431-434, issn 0929-693X, 4 p.Article

Predominant negative symptoms in 22q11.2 deletion syndrome and their associations with cognitive functioning and functional outcomeSCHNEIDER, Maude; VAN DER LINDEN, Martial; MENGHETTI, Sarah et al.Journal of psychiatric research. 2014, Vol 48, Num 1, pp 86-93, issn 0022-3956, 8 p.Article

Quality of Life Among Children With Velocardiofacial SyndromeLOOMAN, Wendy S; THURMES, Anna K; O'CONNER-VON, Susan K et al.The Cleft palate-craniofacial journal. 2010, Vol 47, Num 3, pp 273-283, issn 1055-6656, 11 p.Article

Atypical presentations of 22q11.2 deletion syndrome: explaining the genetic defects and genome architectureTUTULAN-CUNITA, Andreea Cristina; BUDISTEANU, Magdalena; PAPUC, Sorina Mihaela et al.Psychiatry research (Print). 2012, Vol 197, Num 3, pp 356-357, issn 0165-1781, 2 p.Article

Clinically detectable copy number variations in a Canadian catchment population of schizophreniaBASSETT, Anne S; COSTAIN, Gregory; WAILUNALANFUNG et al.Journal of psychiatric research. 2010, Vol 44, Num 15, pp 1005-1009, issn 0022-3956, 5 p.Article

Thyroid Gland and Carotid Artery Anomalies in 22q11.2 Deletion SyndromesDE ALMEIDA, John R; JAMES, Adrian L; PAPSIN, Blake C et al.The Laryngoscope. 2009, Vol 119, Num 8, pp 1495-1500, issn 0023-852X, 6 p.Conference Paper

Clicks Produced as Compensatory Articulations in Two Adolescents With Velocardiofacial SyndromeGIBBON, Fiona; LEE, Alice; YUEN, Ivan et al.The Cleft palate-craniofacial journal. 2008, Vol 45, Num 4, pp 381-392, issn 1055-6656, 12 p.Article

Association of Schizophrenia in 22q11.2 Deletion Syndrome and Gray Matter Volumetric Deficits in the Superior Temporal GyrusCHOW, Eva W. C; HO, Andrew; WEI, Corie et al.The American journal of psychiatry. 2011, Vol 168, Num 5, pp 522-529, issn 0002-953X, 8 p.Article

Craniofacial Morphology in Patients With Velocardiofacial SyndromeDA SILVA DALBEN, Gisele; RICHIERI-COSTA, Antonio; DE ASSIS TAVEIRA, Luis Antônio et al.The Cleft palate-craniofacial journal. 2010, Vol 47, Num 3, pp 241-246, issn 1055-6656, 6 p.Article

Cognitive and Psychiatric Predictors to Psychosis in Velocardiofacial Syndrome: A 3-Year Follow-Up StudyANTSHEL, Kevin M; SHPRINTZEN, Robert; FREMONT, Wanda et al.Journal of the American Academy of Child and Adolescent Psychiatry. 2010, Vol 49, Num 4, pp 333-344, issn 0890-8567, 12 p.Article

Eye Gaze During Face Processing in Children and Adolescents With 22q11.2 Deletion SyndromeGLASER, Bronwyn; DEBBANE, Martin; OTTET, Marie-Christine et al.Journal of the American Academy of Child and Adolescent Psychiatry. 2010, Vol 49, Num 7, pp 665-674, issn 0890-8567, 10 p.Article

Genetic disorders of cardiac morphogenesis : The DiGeorge and velocardiofacial syndromesGOLDMUNTZ, E; EMANUEL, B. S.Circulation research. 1997, Vol 80, Num 4, pp 437-443, issn 0009-7330Article

Social Impairments in Chromosome 22q11.2 Deletion Syndrome (22q11.2DS): Autism Spectrum Disorder or a Different Endophenotype?ANGKUSTSIRI, Kathleen; GOODLIN-JONES, Beth; DEPREY, Lesley et al.Journal of autism and developmental disorders. 2014, Vol 44, Num 4, pp 739-746, issn 0162-3257, 8 p.Article

A Case of Congenitally Absent Left Internal Carotid Artery: Vascular Malformations in 22q11.2 Deletion SyndromeJOHNSON, Matthew D; GENTRY, Lindell R; RICE, Gregory M et al.The Cleft palate-craniofacial journal. 2010, Vol 47, Num 3, pp 314-317, issn 1055-6656, 4 p.Article

The Morphology of the Sella Turcica in Velocardiofacial Syndrome Suggests Involvement of a Neural Crest Developmental FieldMØLSTED, Kirsten; BOERS, Maria; KJÄR, Inger et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 6, pp 1450-1457, issn 1552-4825, 8 p.Article

Monitoring of self-generated speech in adolescents with 22qII.2 deletion syndromeDEBBANE, Martin; VAN DER LINDEN, Martial; GLASER, Bronwyn et al.British journal of clinical psychology. 2010, Vol 49, pp 373-386, issn 0144-6657, 14 p., 3Article

Through-and-Through Dissection of the Soft Palate for High Pharyngeal Flap Inset : A New Technique for the Treatment of Velopharyngeal Incompetence in Velocardiofacial SyndromeARNEJA, Jugpal S; HETTINGER, Patrick; GOSAIN, Arun K et al.Plastic and reconstructive surgery (1963). 2008, Vol 122, Num 3, pp 845-852, issn 0032-1052, 8 p.Article

Unrelated Chromosomal Anomalies Found in Patients With Suspected 22qll.2 DeletionFEMANDEZ, Luis; LAPUNZINA, Pablo; GALAN-GOMEZ, Enrique et al.American journal of medical genetics. Part A. 2008, Vol 146, Num 9, pp 1134-1141, issn 1552-4825, 8 p.Article

MOLECULAR MECHANISMS AND DIAGNOSIS OF CHROMOSOME 22Q11.2 REARRANGEMENTSEMANUEL, Beverly S.Developmental disabilities research reviews. 2008, Vol 14, Num 1, pp 11-18, 8 p.Article

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