-
1
-
-
0038419517
-
A population-based study of the 22q11.2 deletion: Phenotype, incidence, and contribution to major birth defects in the population
-
Botto LD, May K, Fernhoff PM, et al.: A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population. Pediatrics 2003, 112:101-107.
-
(2003)
Pediatrics
, vol.112
, pp. 101-107
-
-
Botto, L.D.1
May, K.2
Fernhoff, P.M.3
-
2
-
-
0842327784
-
Incidence and prevalence of the 22q11 deletion syndrome: A population-based study in Western Sweden
-
Oskarsdottir S, Vujic M, Fasth A: Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden. Arch Dis Child 2004, 89:148-151.
-
(2004)
Arch Dis Child
, vol.89
, pp. 148-151
-
-
Oskarsdottir, S.1
Vujic, M.2
Fasth, A.3
-
3
-
-
22144493861
-
Defining the clinical spectrum of deletion 22q11.2
-
Robin N, Shprintzen RJ: Defining the clinical spectrum of deletion 22q11.2. J Pediatr 2005, 147:90-96.
-
(2005)
J Pediatr
, vol.147
, pp. 90-96
-
-
Robin, N.1
Shprintzen, R.J.2
-
4
-
-
17144376823
-
22Q11.2 deletion syndrome: Genetics, neuroanatomy and cognitive/behavioral features
-
Antshel K, Kates W, Roizen N, et al.: 22Q11.2 deletion syndrome: genetics, neuroanatomy and cognitive/behavioral features. Child Neuropsychol 2005, 11:5-19.
-
(2005)
Child Neuropsychol
, vol.11
, pp. 5-19
-
-
Antshel, K.1
Kates, W.2
Roizen, N.3
-
5
-
-
0026662962
-
Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome
-
Driscoll DA, Spinner NB, Budarf ML, et al.: Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome. Am J Med Genet 1992, 44:261-268.
-
(1992)
Am J Med Genet
, vol.44
, pp. 261-268
-
-
Driscoll, D.A.1
Spinner, N.B.2
Budarf, M.L.3
-
6
-
-
0025796855
-
Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome
-
Scambler PJ, Carey AH, Wyse RK, et al.: Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome. Genomics 1991, 10:201-206.
-
(1991)
Genomics
, vol.10
, pp. 201-206
-
-
Scambler, P.J.1
Carey, A.H.2
Wyse, R.K.3
-
7
-
-
0026511084
-
Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus
-
Scambler PJ, Kelly D, Lindsay E, et al.: Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus. Lancet 1992, 339:1138-1139.
-
(1992)
Lancet
, vol.339
, pp. 1138-1139
-
-
Scambler, P.J.1
Kelly, D.2
Lindsay, E.3
-
8
-
-
85039230838
-
-
Available at:, Accessed December 15
-
Online Mendelian Inheritance in Man #188400. Available at: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=OMIM. Accessed December 15, 2006.
-
(2006)
Online Mendelian Inheritance in Man
, Issue.188400
-
-
-
9
-
-
85039239309
-
-
Available at:, Accessed December 15
-
Online Mendelian Inheritance in Man #192430. Available at: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=OMIM. Accessed December 15, 2006.
-
(2006)
Online Mendelian Inheritance in Man
, Issue.192430
-
-
-
10
-
-
28444441978
-
DiGeorge syndrome: New insights
-
Goldmuntz E: DiGeorge syndrome: new insights. Clin Perinatol 2005, 32:963-978.
-
(2005)
Clin Perinatol
, vol.32
, pp. 963-978
-
-
Goldmuntz, E.1
-
11
-
-
0033837728
-
Dysphagia in children with a 22q11.2 deletion: Unusual pattern found on modified barium swallow
-
Eicher PS, McDonald-Mcginn DM, Fox CA, et al.: Dysphagia in children with a 22q11.2 deletion: unusual pattern found on modified barium swallow. J Pediatr 2000, 137:158-164.
-
(2000)
J Pediatr
, vol.137
, pp. 158-164
-
-
Eicher, P.S.1
McDonald-Mcginn, D.M.2
Fox, C.A.3
-
12
-
-
0034096320
-
The velo-cardio-facial syndrome: A distinctive behavioral phenotype
-
Shprintzen RJ: The velo-cardio-facial syndrome: a distinctive behavioral phenotype. Ment Retard Dev Disabil Res Rev 2001, 6:142-147.
-
(2001)
Ment Retard Dev Disabil Res Rev
, vol.6
, pp. 142-147
-
-
Shprintzen, R.J.1
-
13
-
-
13544259700
-
Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies
-
Beauchesne LM, Warnes CA, Connolly HM, et al.: Prevalence and clinical manifestations of 22q11.2 microdeletion in adults with selected conotruncal anomalies. J Am Coll Cardiol 2005, 45:595-598.
-
(2005)
J Am Coll Cardiol
, vol.45
, pp. 595-598
-
-
Beauchesne, L.M.1
Warnes, C.A.2
Connolly, H.M.3
-
14
-
-
0030122586
-
Schizophrenia, CATCH 22 and FISH
-
Murphy KC, Owen MJ: Schizophrenia, CATCH 22 and FISH. Br J Psychiatry 1996, 168:397-398.
-
(1996)
Br J Psychiatry
, vol.168
, pp. 397-398
-
-
Murphy, K.C.1
Owen, M.J.2
-
15
-
-
0032503887
-
22q11 deletion syndrome in adults with schizophrenia
-
Bassett AS, Hodgkinson K, Chow EW, et al.: 22q11 deletion syndrome in adults with schizophrenia. Am J Med Genet 1998, 81:328-337.
-
(1998)
Am J Med Genet
, vol.81
, pp. 328-337
-
-
Bassett, A.S.1
Hodgkinson, K.2
Chow, E.W.3
-
16
-
-
0032874085
-
22q11 deletion syndrome: A genetic subtype of schizophrenia
-
Bassett AS, Chow EW: 22q11 deletion syndrome: a genetic subtype of schizophrenia. Biol Psychiatry 1999, 46:882-891.
-
(1999)
Biol Psychiatry
, vol.46
, pp. 882-891
-
-
Bassett, A.S.1
Chow, E.W.2
-
18
-
-
0033066999
-
Cognitive and behavioral profile of preschool children with chromosome 22q11.2 deletion
-
Gerdes M, Solot C, Wang PP, et al.: Cognitive and behavioral profile of preschool children with chromosome 22q11.2 deletion. Am J Med Genet 1999, 85:127-133.
-
(1999)
Am J Med Genet
, vol.85
, pp. 127-133
-
-
Gerdes, M.1
Solot, C.2
Wang, P.P.3
-
19
-
-
30944438660
-
The neuropsychological phenotype of velocardiofacial syndrome (VCFS): Relationship to psychopathology
-
Lajiness-O'Neill R, Beaulieu I, Asamoah A, et al.: The neuropsychological phenotype of velocardiofacial syndrome (VCFS): relationship to psychopathology. Arch Clin Neuropsychol 2006, 21:175-184.
-
(2006)
Arch Clin Neuropsychol
, vol.21
, pp. 175-184
-
-
Lajiness-O'Neill, R.1
Beaulieu, I.2
Asamoah, A.3
-
20
-
-
17144423635
-
Neuropsychological characteristics of children with the 22Q11 deletion syndrome: A descriptive analysis
-
Sobin C, Kiley-Brabeck K, Daniels S, et al.: Neuropsychological characteristics of children with the 22Q11 deletion syndrome: a descriptive analysis. Child Neuropsychol 2005, 11:39-53.
-
(2005)
Child Neuropsychol
, vol.11
, pp. 39-53
-
-
Sobin, C.1
Kiley-Brabeck, K.2
Daniels, S.3
-
21
-
-
27644524899
-
COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome
-
Gothelf D, Eliez S, Thompson T, et al.: COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome. Nat Neurosci 2005, 8:1500-1502.
-
(2005)
Nat Neurosci
, vol.8
, pp. 1500-1502
-
-
Gothelf, D.1
Eliez, S.2
Thompson, T.3
-
23
-
-
28444480640
-
Early motor development in young children with 22q.11 deletion syndrome and conotruncal heart defect
-
Swillen A, Feys H, Adriaens T, et al.: Early motor development in young children with 22q.11 deletion syndrome and conotruncal heart defect. Dev Med Child Neurol 2005, 47:797-802.
-
(2005)
Dev Med Child Neurol
, vol.47
, pp. 797-802
-
-
Swillen, A.1
Feys, H.2
Adriaens, T.3
-
24
-
-
0034611998
-
Communication disorders in the 22Q11.2 microdeletion syndrome
-
Solot CB, Knightly C, Handler SD, et al.: Communication disorders in the 22Q11.2 microdeletion syndrome. J Commun Disord 2000, 33:187-203.
-
(2000)
J Commun Disord
, vol.33
, pp. 187-203
-
-
Solot, C.B.1
Knightly, C.2
Handler, S.D.3
-
25
-
-
0031009068
-
Intelligence and psychosocial adjustment in velocardiofacial syndrome: A study of 27 children and adolescents with VCFS
-
Swillen A, Devriendt K, Legius E, et al.: Intelligence and psychosocial adjustment in velocardiofacial syndrome: a study of 27 children and adolescents with VCFS. J Med Genet 1997, 34:453-458.
-
(1997)
J Med Genet
, vol.34
, pp. 453-458
-
-
Swillen, A.1
Devriendt, K.2
Legius, E.3
-
26
-
-
0033361068
-
Neuropsychological, learning, and psychosocial profile of primary school aged children with velo-cardio-facial syndrome (22q11 deletion): Evidence for a nonverbal learning disability?
-
Swillen A, Vandeputte L, Cracco J, et al.: Neuropsychological, learning, and psychosocial profile of primary school aged children with velo-cardio-facial syndrome (22q11 deletion): evidence for a nonverbal learning disability? Child Neuropsychol 1999, 5:230-241.
-
(1999)
Child Neuropsychol
, vol.5
, pp. 230-241
-
-
Swillen, A.1
Vandeputte, L.2
Cracco, J.3
-
27
-
-
84870465485
-
-
American Psychiatric Association:, edn 4. Washington, DC: American Psychiatric Association;
-
American Psychiatric Association: Diagnostic and Statistical Manual of Mental Disorders, edn 4. Washington, DC: American Psychiatric Association; 1994.
-
(1994)
Diagnostic and Statistical Manual of Mental Disorders
-
-
-
28
-
-
17144415267
-
Neuropsychological profile and neuroimaging in patients with 22Q11.2 deletion syndrome: A review
-
Zinkstok J, Amelsvoort T: Neuropsychological profile and neuroimaging in patients with 22Q11.2 deletion syndrome: a review. Child Neuropsychol 2005, 11:21-37.
-
(2005)
Child Neuropsychol
, vol.11
, pp. 21-37
-
-
Zinkstok, J.1
Amelsvoort, T.2
-
29
-
-
0034037817
-
Research on behavioral phenotypes: Velocardiofacial syndrome (deletion 22q11.2)
-
Wang P, Woodin M, Kreps-Falk R, Moss E: Research on behavioral phenotypes: velocardiofacial syndrome (deletion 22q11.2). Dev Med Child Neurol 2000, 42:422-427.
-
(2000)
Dev Med Child Neurol
, vol.42
, pp. 422-427
-
-
Wang, P.1
Woodin, M.2
Kreps-Falk, R.3
Moss, E.4
-
30
-
-
0033063788
-
Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern
-
Moss E, Batshaw M, Solot C, et al.: Psychoeducational profile of the 22q11.2 microdeletion: a complex pattern. J Pediatr 1999, 134:193-198.
-
(1999)
J Pediatr
, vol.134
, pp. 193-198
-
-
Moss, E.1
Batshaw, M.2
Solot, C.3
-
31
-
-
0034873653
-
The neurocognitive phenotype of the 22q11.2 deletion syndrome: Selective deficit in visual-spatial memory
-
Bearden CE, Woodin MF, Wang PP: The neurocognitive phenotype of the 22q11.2 deletion syndrome: selective deficit in visual-spatial memory. J Clin Exp Neuropsychol 2001, 23:447-464.
-
(2001)
J Clin Exp Neuropsychol
, vol.23
, pp. 447-464
-
-
Bearden, C.E.1
Woodin, M.F.2
Wang, P.P.3
-
32
-
-
0035746483
-
Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion
-
Woodin M, Wang P, Aleman D, et al.: Neuropsychological profile of children and adolescents with the 22q11.2 microdeletion. Genet Med 2001, 3:34-39.
-
(2001)
Genet Med
, vol.3
, pp. 34-39
-
-
Woodin, M.1
Wang, P.2
Aleman, D.3
-
33
-
-
4344619866
-
Cognitive deficits associated with schizophrenia in velo-cardio-facial syndrome
-
van Amelsvoort T, Henry J, Morris R, et al.: Cognitive deficits associated with schizophrenia in velo-cardio-facial syndrome. Schizophr Res 2004, 70:223-232.
-
(2004)
Schizophr Res
, vol.70
, pp. 223-232
-
-
van Amelsvoort, T.1
Henry, J.2
Morris, R.3
-
34
-
-
24044515278
-
Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome
-
Fine SE, Weissman A, Gerdes M, et al.: Autism spectrum disorders and symptoms in children with molecularly confirmed 22q11.2 deletion syndrome. J Autism Dev Disord 2005, 35:461-470.
-
(2005)
J Autism Dev Disord
, vol.35
, pp. 461-470
-
-
Fine, S.E.1
Weissman, A.2
Gerdes, M.3
-
35
-
-
0035746376
-
Neuropsychiatric disorders in the 22q11 deletion syndrome
-
Niklasson L, Rasmussen P, Oskarsdottir S, Gillberg C: Neuropsychiatric disorders in the 22q11 deletion syndrome. Genet Med 2001, 3:79-84.
-
(2001)
Genet Med
, vol.3
, pp. 79-84
-
-
Niklasson, L.1
Rasmussen, P.2
Oskarsdottir, S.3
Gillberg, C.4
-
36
-
-
33748426974
-
The 22q11.2 deletion in children: High rate of autistic disorders and early onset of psychotic symptoms
-
Vorstman JA, Morcus ME, Duijff SN, et al.: The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms. J Am Acad Child Adolesc Psychiatry 2006, 45:1104-1112.
-
(2006)
J Am Acad Child Adolesc Psychiatry
, vol.45
, pp. 1104-1112
-
-
Vorstman, J.A.1
Morcus, M.E.2
Duijff, S.N.3
-
37
-
-
34147200502
-
Autistic spectrum disorders in velo-cardio facial syndrome (22q11.2 deletion)
-
Epub ahead of print
-
Antshel KM, Aneja A, Strunge L, et al.: Autistic spectrum disorders in velo-cardio facial syndrome (22q11.2 deletion). J Autism Dev Disord 2006 [Epub ahead of print].
-
(2006)
J Autism Dev Disord
-
-
Antshel, K.M.1
Aneja, A.2
Strunge, L.3
-
38
-
-
33645559153
-
Prevalence of ADHD in children with velocardiofacial syndrome: A preliminary report
-
Zagursky K, Weller RA, Jessani N, et al.: Prevalence of ADHD in children with velocardiofacial syndrome: a preliminary report. Curr Psychiatry Rep 2006, 8:102-107.
-
(2006)
Curr Psychiatry Rep
, vol.8
, pp. 102-107
-
-
Zagursky, K.1
Weller, R.A.2
Jessani, N.3
-
40
-
-
0035085859
-
Genetics of childhood disorders: XXV. Velocardiofacial syndrome
-
Gothelf D, Lombroso PJ: Genetics of childhood disorders: XXV. Velocardiofacial syndrome. J Am Acad Child Adolesc Psychiatry 2001, 40:489-491.
-
(2001)
J Am Acad Child Adolesc Psychiatry
, vol.40
, pp. 489-491
-
-
Gothelf, D.1
Lombroso, P.J.2
-
41
-
-
0037084412
-
Psychiatric disorders and behavioral problems in children with velocardiofacial syndrome: Usefulness as phenotypic indicators of schizophrenia risk
-
Feinstein C, Eliez S, Blasey C, Reiss AL: Psychiatric disorders and behavioral problems in children with velocardiofacial syndrome: usefulness as phenotypic indicators of schizophrenia risk. Biol Psychiatry 2002, 51:312-318.
-
(2002)
Biol Psychiatry
, vol.51
, pp. 312-318
-
-
Feinstein, C.1
Eliez, S.2
Blasey, C.3
Reiss, A.L.4
-
42
-
-
0032882849
-
High rates of schizophrenia in adults with velo-cardio-facial syndrome
-
Murphy K, Jone L, Owen M: High rates of schizophrenia in adults with velo-cardio-facial syndrome. Arch Gen Psychiatry 1999, 56:940-945.
-
(1999)
Arch Gen Psychiatry
, vol.56
, pp. 940-945
-
-
Murphy, K.1
Jone, L.2
Owen, M.3
-
43
-
-
19744372613
-
Prevalence of intellectual disability and comorbid mental illness in an Australian community sample
-
White P, Chant D, Edwards N, et al.: Prevalence of intellectual disability and comorbid mental illness in an Australian community sample. Aust N Z J Psychiatry 2005, 39:395-400.
-
(2005)
Aust N Z J Psychiatry
, vol.39
, pp. 395-400
-
-
White, P.1
Chant, D.2
Edwards, N.3
-
44
-
-
0032874313
-
Aggressive behavior in patients with attention-deficit/hyperactivity disorder, conduct disorder, and pervasive developmental disorders
-
Weller EB, Rowan A, Elia J, Weller RA: Aggressive behavior in patients with attention-deficit/hyperactivity disorder, conduct disorder, and pervasive developmental disorders. J Clin Psychiatry 1999, 60(Suppl 15):5-11.
-
(1999)
J Clin Psychiatry
, vol.60
, Issue.SUPPL. 15
, pp. 5-11
-
-
Weller, E.B.1
Rowan, A.2
Elia, J.3
Weller, R.A.4
-
45
-
-
3142767559
-
Genetic abnormalities of chromosome 22 and the development of psychosis
-
Williams NM, Owen MJ: Genetic abnormalities of chromosome 22 and the development of psychosis. Curr Psychiatry Rep 2004, 6:176-182.
-
(2004)
Curr Psychiatry Rep
, vol.6
, pp. 176-182
-
-
Williams, N.M.1
Owen, M.J.2
-
46
-
-
13244261075
-
Adolescents and young adults with 22q11 deletion syndrome: Psychopathology in an at-risk group
-
Baker KD, Skuse DH: Adolescents and young adults with 22q11 deletion syndrome: psychopathology in an at-risk group. Br J Psychol 2005, 186:115-120.
-
(2005)
Br J Psychol
, vol.186
, pp. 115-120
-
-
Baker, K.D.1
Skuse, D.H.2
-
47
-
-
33747485290
-
Psychotic symptoms in children and adolescents with 22q11.2 deletion syndrome: Neuropsychological and behavioral implications
-
Debbane M, Glaser B, David MK, et al.: Psychotic symptoms in children and adolescents with 22q11.2 deletion syndrome: neuropsychological and behavioral implications. Schizophr Res 2006, 84:187-193.
-
(2006)
Schizophr Res
, vol.84
, pp. 187-193
-
-
Debbane, M.1
Glaser, B.2
David, M.K.3
-
48
-
-
0037045148
-
The New York high risk project to the Hillside recognition and prevention (RAP) program
-
Cornblatt BA: The New York high risk project to the Hillside recognition and prevention (RAP) program. Am J Med Genet 2002, 114:956-966.
-
(2002)
Am J Med Genet
, vol.114
, pp. 956-966
-
-
Cornblatt, B.A.1
-
49
-
-
0034616254
-
Can we improve the diagnostic efficiency and predictive power of prodromal symptoms of schizophrenia?
-
McGorry PD, McKenzie D, Jackson HJ, et al.: Can we improve the diagnostic efficiency and predictive power of prodromal symptoms of schizophrenia? Schizophr Res 2000, 42:91-100.
-
(2000)
Schizophr Res
, vol.42
, pp. 91-100
-
-
McGorry, P.D.1
McKenzie, D.2
Jackson, H.J.3
-
50
-
-
0030910606
-
Molecular analysis of velo-cardio-facial syndrome in patients with psychiatric disorders
-
Carlson C, Papolos D, Pandita RK, et al.: Molecular analysis of velo-cardio-facial syndrome in patients with psychiatric disorders. Am J Hum Genet 1997, 60:851-859.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 851-859
-
-
Carlson, C.1
Papolos, D.2
Pandita, R.K.3
-
51
-
-
0035826540
-
Velo-cardio-facial syndrome: Implications of microdeletion 22q11 for schizophrenia and mood disorders
-
Arnold PD, Siegel-Bartelt J, Cytrynbaum C, et al.: Velo-cardio-facial syndrome: implications of microdeletion 22q11 for schizophrenia and mood disorders. Am J Med Genet 2001, 105:354-362.
-
(2001)
Am J Med Genet
, vol.105
, pp. 354-362
-
-
Arnold, P.D.1
Siegel-Bartelt, J.2
Cytrynbaum, C.3
-
52
-
-
0029853761
-
Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: Does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?
-
Papolos DF, Faedda GL, Veit S, et al.: Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: Does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder? Am J Psychiatry 1996, 153:1541-1547.
-
(1996)
Am J Psychiatry
, vol.153
, pp. 1541-1547
-
-
Papolos, D.F.1
Faedda, G.L.2
Veit, S.3
-
53
-
-
0027989917
-
Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives
-
Pulver AE, Nestadt G, Goldberg R, et al.: Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives. J Nerv Ment Dis 1994, 182:476-478.
-
(1994)
J Nerv Ment Dis
, vol.182
, pp. 476-478
-
-
Pulver, A.E.1
Nestadt, G.2
Goldberg, R.3
-
54
-
-
33646755589
-
ADHD, major depressive disorder, and simple phobias are prevalent psychiatric conditions in youth with velocardiofacial syndrome
-
Antshel KM, Fremont W, Roizen NJ, et al.: ADHD, major depressive disorder, and simple phobias are prevalent psychiatric conditions in youth with velocardiofacial syndrome. J Am Acad Child Adolesc Psychiatry 2006, 45:596-603.
-
(2006)
J Am Acad Child Adolesc Psychiatry
, vol.45
, pp. 596-603
-
-
Antshel, K.M.1
Fremont, W.2
Roizen, N.J.3
-
55
-
-
0035746533
-
Taking advantage of early diagnosis: Preschool children with the 22q11.2 deletion
-
Gerdes M, Solot C, Wang P, et al.: Taking advantage of early diagnosis: preschool children with the 22q11.2 deletion. Genet Med 2001, 3:40-44.
-
(2001)
Genet Med
, vol.3
, pp. 40-44
-
-
Gerdes, M.1
Solot, C.2
Wang, P.3
-
56
-
-
0035746362
-
Communication issues in 22q11.2 deletion syndrome: Children at risk
-
Solot C, Gerdes M, Kirschner R, et al.: Communication issues in 22q11.2 deletion syndrome: children at risk. Genet Med 2001, 3:67-71.
-
(2001)
Genet Med
, vol.3
, pp. 67-71
-
-
Solot, C.1
Gerdes, M.2
Kirschner, R.3
-
57
-
-
0031989472
-
Early intervention and early experience
-
Ramey C, Ramey SL: Early intervention and early experience. Am Psychol 1998, 53:109-120.
-
(1998)
Am Psychol
, vol.53
, pp. 109-120
-
-
Ramey, C.1
Ramey, S.L.2
-
58
-
-
0035209099
-
Predicting spoken language level in children with autism spectrum disorders
-
Stone WL, Yoder PJ: Predicting spoken language level in children with autism spectrum disorders. Autism 2001, 5:341-361.
-
(2001)
Autism
, vol.5
, pp. 341-361
-
-
Stone, W.L.1
Yoder, P.J.2
-
60
-
-
33745770485
-
Health, education, work, and independence of young adults with disabilities
-
Blomquist KB: Health, education, work, and independence of young adults with disabilities. Orthop Nurs 2006, 25:168-187.
-
(2006)
Orthop Nurs
, vol.25
, pp. 168-187
-
-
Blomquist, K.B.1
-
61
-
-
0033545227
-
Clinical characteristics of schizophrenia associated with velo-cardio-facial syndrome
-
Gothelf D, Frisch A, Munitz H, et al.: Clinical characteristics of schizophrenia associated with velo-cardio-facial syndrome. Schizophr Res 1999, 35:105-112.
-
(1999)
Schizophr Res
, vol.35
, pp. 105-112
-
-
Gothelf, D.1
Frisch, A.2
Munitz, H.3
-
62
-
-
33747485290
-
Psychotic symptoms in children and adolescents with 22q11.2 deletion syndrome: Neuropsychological and behavioral implications
-
Debbane M, Glaser B, David MK, et al.: Psychotic symptoms in children and adolescents with 22q11.2 deletion syndrome: neuropsychological and behavioral implications. Schizophr Res 2006, 84:187-193.
-
(2006)
Schizophr Res
, vol.84
, pp. 187-193
-
-
Debbane, M.1
Glaser, B.2
David, M.K.3
-
63
-
-
0031893397
-
Thyroid abnormalities as a feature of DiGeorge syndrome: A patient report and review of the literature
-
Scuccimarri R, Rodd C: Thyroid abnormalities as a feature of DiGeorge syndrome: a patient report and review of the literature. J Pediatr Endocrinol Metab 1998, 11:273-276.
-
(1998)
J Pediatr Endocrinol Metab
, vol.11
, pp. 273-276
-
-
Scuccimarri, R.1
Rodd, C.2
-
64
-
-
20344394935
-
Annotation: Velo-cardio-facial syndrome
-
Murphy KC: Annotation: velo-cardio-facial syndrome. J Child Psychol Psychiatry 2005, 46:563-571.
-
(2005)
J Child Psychol Psychiatry
, vol.46
, pp. 563-571
-
-
Murphy, K.C.1
-
65
-
-
0029853761
-
Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: Does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?
-
Papolos DF, Faedda GL, Veit S, et al.: Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: Does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder? Am J Psychiatry 1996, 153:1541-1547.
-
(1996)
Am J Psychiatry
, vol.153
, pp. 1541-1547
-
-
Papolos, D.F.1
Faedda, G.L.2
Veit, S.3
-
66
-
-
12144289483
-
Obsessive-compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome
-
Gothelf D, Presburger G, Zohar AH, et al.: Obsessive-compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome. Am J Med Genet B Neuropsychiatr Genet 2004, 126:99-105.
-
(2004)
Am J Med Genet B Neuropsychiatr Genet
, vol.126
, pp. 99-105
-
-
Gothelf, D.1
Presburger, G.2
Zohar, A.H.3
-
67
-
-
0029102665
-
Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11
-
Karayiorgou M, Morris MA, Morrow B, et al.: Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11. Proc Natl Acad Sci U S A 1995, 92:7612-7616.
-
(1995)
Proc Natl Acad Sci U S A
, vol.92
, pp. 7612-7616
-
-
Karayiorgou, M.1
Morris, M.A.2
Morrow, B.3
|