-
1
-
-
0004235298
-
-
American Psychiatric Association , 4th ed. Text revision. Washington, DC: American Psychiatric Association
-
American Psychiatric Association (2000). Diagnostic and statistical manual of mental disorders DSM-IV-TR. 4th ed. Text revision. Washington, DC: American Psychiatric Association.
-
(2000)
Diagnostic and statistical manual of mental disorders DSM-IV-TR
-
-
-
2
-
-
0034583691
-
Saethre-Chotzen syndrome: Review of the literature and report of a case
-
Clauser L, Galie M, Hassanipour A, Calabrese O (2000). Saethre-Chotzen syndrome: review of the literature and report of a case. J Craniofac Surg 11:480-486.
-
(2000)
J Craniofac Surg
, vol.11
, pp. 480-486
-
-
Clauser, L.1
Galie, M.2
Hassanipour, A.3
Calabrese, O.4
-
3
-
-
20044385411
-
Clinical and genetic analysis of patients with Saethre-Chotzen syndrome
-
De Heer IM, de Klein A, van den Ouweland AM, Vermeij-Keers C, Wouters CH, Vaandrager JM, et al. (2005). Clinical and genetic analysis of patients with Saethre-Chotzen syndrome. Plast Reconstr Surg 115:1894-1902.
-
(2005)
Plast Reconstr Surg
, vol.115
, pp. 1894-1902
-
-
De Heer, I.M.1
de Klein, A.2
van den Ouweland, A.M.3
Vermeij-Keers, C.4
Wouters, C.H.5
Vaandrager, J.M.6
-
4
-
-
33748076432
-
Attention-deficit hyperactivity disorder (ADHD) comorbidity: A case for 'pure' Tourette syndrome?
-
Denckla MB (2006). Attention-deficit hyperactivity disorder (ADHD) comorbidity: a case for 'pure' Tourette syndrome? J Child Neurol 21:701-703.
-
(2006)
J Child Neurol
, vol.21
, pp. 701-703
-
-
Denckla, M.B.1
-
5
-
-
0026503780
-
Neuropsychiatric manifestations of Saethre-Chotzen syndrome]
-
Fehlow P, Frohlich B, Miosge W, Otto W, Walther F (1992). [Neuropsychiatric manifestations of Saethre-Chotzen syndrome]. Fortschr Neurol Psychiatr 60:66-73.
-
(1992)
Fortschr Neurol Psychiatr
, vol.60
, pp. 66-73
-
-
Fehlow, P.1
Frohlich, B.2
Miosge, W.3
Otto, W.4
Walther, F.5
-
6
-
-
0032231374
-
A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1
-
Johnson D, Horsley SW, Moloney DM, Oldridge M, Twigg SR, Walsh S, et al. (1998). A comprehensive screen for TWIST mutations in patients with craniosynostosis identifies a new microdeletion syndrome of chromosome band 7p21.1. Am J Hum Genet 63:1282-1293.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1282-1293
-
-
Johnson, D.1
Horsley, S.W.2
Moloney, D.M.3
Oldridge, M.4
Twigg, S.R.5
Walsh, S.6
-
7
-
-
0029865979
-
Case study: Comorbidity among Tourette's syndrome, autistic disorder, and bipolar disorder
-
Kerbeshian J, Burd L (1996). Case study: comorbidity among Tourette's syndrome, autistic disorder, and bipolar disorder. J Am Acad Child Adolesc Psychiatry 35:681-685.
-
(1996)
J Am Acad Child Adolesc Psychiatry
, vol.35
, pp. 681-685
-
-
Kerbeshian, J.1
Burd, L.2
-
8
-
-
0028819689
-
Comorbid Tourette's disorder and bipolar disorder: An etiologic perspective
-
Kerbeshian J, Burd L, Klug MG (1995). Comorbid Tourette's disorder and bipolar disorder: an etiologic perspective. Am J Psychiatry 152:1646-1651.
-
(1995)
Am J Psychiatry
, vol.152
, pp. 1646-1651
-
-
Kerbeshian, J.1
Burd, L.2
Klug, M.G.3
-
9
-
-
0034615073
-
Peek-a-boo fragile site at 16d associated with Tourette syndrome, bipolar disorder, autistic disorder, and mental retardation
-
Kerbeshian J, Severud R, Burd L, Larson L (2000). Peek-a-boo fragile site at 16d associated with Tourette syndrome, bipolar disorder, autistic disorder, and mental retardation. Am J Med Genet 96:69-73.
-
(2000)
Am J Med Genet
, vol.96
, pp. 69-73
-
-
Kerbeshian, J.1
Severud, R.2
Burd, L.3
Larson, L.4
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