-
1
-
-
0034645510
-
Cognitive and behavioral profile of fragile X boys: Correlations to molecular data
-
Backes M, Genc B, Schreck J, Doerfler W, Lehmkuhl G, von Gontard A. 2000. Cognitive and behavioral profile of fragile X boys: Correlations to molecular data. Am J Med Genet 95:150-156.
-
(2000)
Am J Med Genet
, vol.95
, pp. 150-156
-
-
Backes, M.1
Genc, B.2
Schreck, J.3
Doerfler, W.4
Lehmkuhl, G.5
von Gontard, A.6
-
2
-
-
0015831045
-
A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies
-
Cohen MM Jr, Hall BD, Smith DW, Graham CB, Lampert KJ. 1973. A new syndrome with hypotonia, obesity, mental deficiency, and facial, oral, ocular, and limb anomalies. J Pediatr 83:280-284.
-
(1973)
J Pediatr
, vol.83
, pp. 280-284
-
-
Cohen Jr, M.M.1
Hall, B.D.2
Smith, D.W.3
Graham, C.B.4
Lampert, K.J.5
-
3
-
-
0036948994
-
X-linked mental retardation: Vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms
-
Frints SG, Froyen G, Marynen P, Fryns JP. 2002. X-linked mental retardation: Vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms. Clin Genet 62:423-432.
-
(2002)
Clin Genet
, vol.62
, pp. 423-432
-
-
Frints, S.G.1
Froyen, G.2
Marynen, P.3
Fryns, J.P.4
-
4
-
-
0041823333
-
X-linked mild non-syndromic mental retardation with neuropsychiatric problems and the missense mutation A365E in P AK3
-
Gedeon AK, Nelson J, Gecz J, Mulley JC. 2003. X-linked mild non-syndromic mental retardation with neuropsychiatric problems and the missense mutation A365E in P AK3. Am J Med Genet Part A 120A:509-517.
-
(2003)
Am J Med Genet
, vol.120 A
, Issue.PART A
, pp. 509-517
-
-
Gedeon, A.K.1
Nelson, J.2
Gecz, J.3
Mulley, J.C.4
-
5
-
-
12144289483
-
-
Gothelf D, Presburger G, Zohar AH, Burg M, Nahmani A, Frydman M, Shohat M, Inbar D, Aviram-Goldring A, Yeshaya J, Steinberg T, Finkelstein Y, Frisch A, Weizman A, Apter A. 2004. Obsessive-compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome. Am J Med Genet Part B Neuropsychiatr Genet 126B:99-105.
-
Gothelf D, Presburger G, Zohar AH, Burg M, Nahmani A, Frydman M, Shohat M, Inbar D, Aviram-Goldring A, Yeshaya J, Steinberg T, Finkelstein Y, Frisch A, Weizman A, Apter A. 2004. Obsessive-compulsive disorder in patients with velocardiofacial (22q11 deletion) syndrome. Am J Med Genet Part B Neuropsychiatr Genet 126B:99-105.
-
-
-
-
6
-
-
0016809496
-
The KBG syndrome - a syndrome of short stature, characteristic fades, mental retardation, macrodontia and skeletal anomalies
-
Herrmann J, Pallister PD, Tiddy W, Opitz JM. 1975. The KBG syndrome - a syndrome of short stature, characteristic fades, mental retardation, macrodontia and skeletal anomalies. Birth Defects Orig Artic Ser 11:7-18.
-
(1975)
Birth Defects Orig Artic Ser
, vol.11
, pp. 7-18
-
-
Herrmann, J.1
Pallister, P.D.2
Tiddy, W.3
Opitz, J.M.4
-
7
-
-
0036948248
-
The epidemiology of mental retardation: Challenges and opportunities in the new millennium
-
Leonard H, Wen X. 2002. The epidemiology of mental retardation: Challenges and opportunities in the new millennium. Ment Retard Dev Disabil Res Rev 8:117-134.
-
(2002)
Ment Retard Dev Disabil Res Rev
, vol.8
, pp. 117-134
-
-
Leonard, H.1
Wen, X.2
-
8
-
-
0019219903
-
Short stature, psychomotor retardation, and unusual facial appearance in two brothers
-
Smith RD, Fineman RM, Myers GG. 1980. Short stature, psychomotor retardation, and unusual facial appearance in two brothers. Am J Med Genet 7:5-9.
-
(1980)
Am J Med Genet
, vol.7
, pp. 5-9
-
-
Smith, R.D.1
Fineman, R.M.2
Myers, G.G.3
-
9
-
-
21344455303
-
20051 Etiology of mental retardation in children referred to a tertiary care center: A prospective study
-
Van Karnebeek CD, Scheper FY, Abeling NG, Alders M, Barth PG, Hoovers JM, Koevoets C, Wanders RJ, Hennekam RC. 20051 Etiology of mental retardation in children referred to a tertiary care center: A prospective study. Am J Ment Retard 110:253-267.
-
Am J Ment Retard
, vol.110
, pp. 253-267
-
-
Van Karnebeek, C.D.1
Scheper, F.Y.2
Abeling, N.G.3
Alders, M.4
Barth, P.G.5
Hoovers, J.M.6
Koevoets, C.7
Wanders, R.J.8
Hennekam, R.C.9
-
10
-
-
0033624906
-
Identification of a mutation in the XNP/ATR-X gene in a family reported as Smith-Fineman-Myers syndrome
-
Villard L, Fontes M, Ades LC, Gecz J. 2000. Identification of a mutation in the XNP/ATR-X gene in a family reported as Smith-Fineman-Myers syndrome. Am J Med Genet 91: 83-85.
-
(2000)
Am J Med Genet
, vol.91
, pp. 83-85
-
-
Villard, L.1
Fontes, M.2
Ades, L.C.3
Gecz, J.4
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