593 related articles for article (PubMed ID: 15181786)
41. The Philadelphia story: the 22q11.2 deletion: report on 250 patients.
McDonald-McGinn DM; Kirschner R; Goldmuntz E; Sullivan K; Eicher P; Gerdes M; Moss E; Solot C; Wang P; Jacobs I; Handler S; Knightly C; Heher K; Wilson M; Ming JE; Grace K; Driscoll D; Pasquariello P; Randall P; Larossa D; Emanuel BS; Zackai EH
Genet Couns; 1999; 10(1):11-24. PubMed ID: 10191425
[TBL] [Abstract][Full Text] [Related]
42. Clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experience.
Vantrappen G; Rommel N; Devriendt K; Cremers CW; Feenstra L; Fryns JP
Acta Otorhinolaryngol Belg; 2001; 55(1):43-8. PubMed ID: 11256191
[TBL] [Abstract][Full Text] [Related]
43. Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome.
Fine SE; Weissman A; Gerdes M; Pinto-Martin J; Zackai EH; McDonald-McGinn DM; Emanuel BS
J Autism Dev Disord; 2005 Aug; 35(4):461-70. PubMed ID: 16134031
[TBL] [Abstract][Full Text] [Related]
44. 22q11 deletion syndrome in adults with schizophrenia.
Bassett AS; Hodgkinson K; Chow EW; Correia S; Scutt LE; Weksberg R
Am J Med Genet; 1998 Jul; 81(4):328-37. PubMed ID: 9674980
[TBL] [Abstract][Full Text] [Related]
45. Risk of Psychiatric Disorders Among Individuals With the 22q11.2 Deletion or Duplication: A Danish Nationwide, Register-Based Study.
Hoeffding LK; Trabjerg BB; Olsen L; Mazin W; Sparsø T; Vangkilde A; Mortensen PB; Pedersen CB; Werge T
JAMA Psychiatry; 2017 Mar; 74(3):282-290. PubMed ID: 28114601
[TBL] [Abstract][Full Text] [Related]
46. [Significant progress in the genetic origin of Martin-Bell syndrome including diagnostic consequences].
Hebebrand J; Warnke A; Remschmidt H
Z Kinder Jugendpsychiatr; 1992 Sep; 20(3):197-202. PubMed ID: 1414026
[No Abstract] [Full Text] [Related]
47. Autism, ADHD, mental retardation and behavior problems in 100 individuals with 22q11 deletion syndrome.
Niklasson L; Rasmussen P; Oskarsdóttir S; Gillberg C
Res Dev Disabil; 2009; 30(4):763-73. PubMed ID: 19070990
[TBL] [Abstract][Full Text] [Related]
48. Phenotype of adults with the 22q11 deletion syndrome: A review.
Cohen E; Chow EW; Weksberg R; Bassett AS
Am J Med Genet; 1999 Oct; 86(4):359-65. PubMed ID: 10494092
[TBL] [Abstract][Full Text] [Related]
49. PDD-NOS, psychotic features and executive function deficits in a boy with proximal 22q11.2 microduplication: Evolution of the psychiatric symptom profile from childhood to adolescence.
Woestelandt L; Novo A; Philippe A; Guyaux N; Rio M; Romano S; Robel L
Eur J Med Genet; 2018 May; 61(5):280-283. PubMed ID: 29307791
[TBL] [Abstract][Full Text] [Related]
50. [22q11 deletion syndrome: an expanding phenotype].
Moreno Izco F; Zuazo Zamalloa E; González Alvaredo S; Bereciartu Irastorza P
Neurologia; 2009; 24(1):69-71. PubMed ID: 19214819
[TBL] [Abstract][Full Text] [Related]
51. Deep psychophysiological phenotyping of adolescents and adults with 22q11.2 deletion syndrome: a multilevel approach to defining core disease processes.
Parker DA; Cubells JF; Imes SL; Ruban GA; Henshey BT; Massa NM; Walker EF; Duncan EJ; Ousley OY
BMC Psychiatry; 2023 Jun; 23(1):425. PubMed ID: 37312091
[TBL] [Abstract][Full Text] [Related]
52. Is the autosomal dominant Optiz GBBB syndrome part of the DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2?
Wulfsberg EA
Am J Med Genet; 1996 Aug; 64(3):523-4. PubMed ID: 8862634
[No Abstract] [Full Text] [Related]
53. The 22q11.2 deletion syndrome.
Emanuel BS; McDonald-McGinn D; Saitta SC; Zackai EH
Adv Pediatr; 2001; 48():39-73. PubMed ID: 11480765
[TBL] [Abstract][Full Text] [Related]
54. Terminal 2q37 deletion and autistic behaviour.
Lukusa T; Smeets E; Vogels A; Vermeesch JR; Fryns JP
Genet Couns; 2005; 16(2):179-80. PubMed ID: 16080299
[No Abstract] [Full Text] [Related]
55. Presenting phenotype in 100 children with the 22q11 deletion syndrome.
Oskarsdóttir S; Persson C; Eriksson BO; Fasth A
Eur J Pediatr; 2005 Mar; 164(3):146-53. PubMed ID: 15565286
[TBL] [Abstract][Full Text] [Related]
56. [22q11.2 chromosome deletion and velo-cardio-facial syndrome in a patient with tetralogy of Fallot].
Morava E; Masszi G; Czakó M; Tóth G; Melegh B; Kosztolányi G
Orv Hetil; 2000 Aug; 141(34):1873-5. PubMed ID: 11006712
[TBL] [Abstract][Full Text] [Related]
57. Craniofacial dysmorphology in 22q11.2 deletion syndrome by 3D laser surface imaging and geometric morphometrics: illuminating the developmental relationship to risk for psychosis.
Prasad S; Katina S; Hennessy RJ; Murphy KC; Bowman AW; Waddington JL
Am J Med Genet A; 2015 Mar; 167A(3):529-36. PubMed ID: 25691406
[TBL] [Abstract][Full Text] [Related]
58. TWINS WITH KLEEFSTRA SYNDROME DUE TO CHROMOSOME 9q34.3 MICRODELETION.
Atik T; Karaca E; Ozkinay E; Cogulu O
Genet Couns; 2015; 26(4):431-5. PubMed ID: 26852514
[TBL] [Abstract][Full Text] [Related]
59. [22q11.2 deletion and schizophrenia in childhood and adolescence].
Briegel W
Z Kinder Jugendpsychiatr Psychother; 2007 Sep; 35(5):353-7; quiz 357-8. PubMed ID: 18074829
[TBL] [Abstract][Full Text] [Related]
60. Psychiatric disorders from childhood to adulthood in 22q11.2 deletion syndrome: results from the International Consortium on Brain and Behavior in 22q11.2 Deletion Syndrome.
Schneider M; Debbané M; Bassett AS; Chow EW; Fung WL; van den Bree M; Owen M; Murphy KC; Niarchou M; Kates WR; Antshel KM; Fremont W; McDonald-McGinn DM; Gur RE; Zackai EH; Vorstman J; Duijff SN; Klaassen PW; Swillen A; Gothelf D; Green T; Weizman A; Van Amelsvoort T; Evers L; Boot E; Shashi V; Hooper SR; Bearden CE; Jalbrzikowski M; Armando M; Vicari S; Murphy DG; Ousley O; Campbell LE; Simon TJ; Eliez S;
Am J Psychiatry; 2014 Jun; 171(6):627-39. PubMed ID: 24577245
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]