-
1
-
-
0028220536
-
An examination of linkage of schizophrenia and schizoafffective disorder to the pseudoautosomal region (Xp22.3)
-
Crow TJ, DeLisi LE, Lofthouse R, Poulter M, Lehner T, Bass N, et al. (1994). An examination of linkage of schizophrenia and schizoafffective disorder to the pseudoautosomal region (Xp22.3). Br J Psy 164:159-164.
-
(1994)
Br J Psy
, vol.164
, pp. 159-164
-
-
Crow, T.J.1
DeLisi, L.E.2
Lofthouse, R.3
Poulter, M.4
Lehner, T.5
Bass, N.6
-
2
-
-
0027314753
-
Characteristic facial dysmorphism, arachnodactyly and mental handicap in two unrelated girls: A distinct MCA/ MR syndrome?
-
de Die-Smulders C, Vies H, Fryns JP (1990). Characteristic facial dysmorphism, arachnodactyly and mental handicap in two unrelated girls: A distinct MCA/ MR syndrome? Genet Couns 4:165-167.
-
(1990)
Genet Couns
, vol.4
, pp. 165-167
-
-
De Die-Smulders, C.1
Vies, H.2
Fryns, J.P.3
-
3
-
-
0029995113
-
Lujan-Fryns syndrome in the differential diagnosis of schizophrenia
-
De Hert M, Steemans D, Theys P, Fryns JP, Peuskens J (1996). Lujan-Fryns syndrome in the differential diagnosis of schizophrenia. Am J Med Genet 67:212-214.
-
(1996)
Am J Med Genet
, vol.67
, pp. 212-214
-
-
De Hert, M.1
Steemans, D.2
Theys, P.3
Fryns, J.P.4
Peuskens, J.5
-
4
-
-
18744432779
-
Failure to establish linkage on the X chromosome in 301 families with schizophrenia or schizoaffective disorder
-
DeLisi LE, Shaw S, Sherrington R, Nanthakumar B, Shields G, Smith AB, et al. (2000). Failure to establish linkage on the X chromosome in 301 families with schizophrenia or schizoaffective disorder. Am J Med Genet 96:335-341.
-
(2000)
Am J Med Genet
, vol.96
, pp. 335-341
-
-
DeLisi, L.E.1
Shaw, S.2
Sherrington, R.3
Nanthakumar, B.4
Shields, G.5
Smith, A.B.6
-
5
-
-
0037154033
-
Preserved neurobehavioural abilities in Lujan-Fryns syndrome
-
Donders J, Toriello H, Van Doornik S (2002). Preserved neurobehavioural abilities in Lujan-Fryns syndrome. Am J Med Genet 107:243-246.
-
(2002)
Am J Med Genet
, vol.107
, pp. 243-246
-
-
Donders, J.1
Toriello, H.2
Van Doornik, S.3
-
6
-
-
0027209748
-
Mental retardation with marfanoid syndrome: Presentation of a family with different phenotypical expression
-
Dotti MT, Malandrini A, Bartolini S, Fabrizi GM, Federico A (1993). Mental retardation with marfanoid syndrome: presentation of a family with different phenotypical expression. Brain Dev 15:291-294.
-
(1993)
Brain Dev
, vol.15
, pp. 291-294
-
-
Dotti, M.T.1
Malandrini, A.2
Bartolini, S.3
Fabrizi, G.M.4
Federico, A.5
-
7
-
-
0001886378
-
Behavioural phenotypes
-
Rutter M, Taylor E, Hersov L (editors). Oxford: Blackwell Scientific
-
Flint J, Yule W (1994). Behavioural phenotypes. In: Rutter M, Taylor E, Hersov L (editors). Child adolescent psychiatry. 3rd edn. Oxford: Blackwell Scientific; pp. 666-687.
-
(1994)
Child Adolescent Psychiatry. 3rd Edn.
, pp. 666-687
-
-
Flint, J.1
Yule, W.2
-
8
-
-
0036948994
-
X-linked mental retardation: Vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms
-
Prints SGM, Froyen G, Marynen P, Fryns J-P (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
-
-
Prints, S.G.M.1
Froyen, G.2
Marynen, P.3
Fryns, J.-P.4
-
9
-
-
0026008095
-
X-linked mental retardation with marfanoid habitus
-
Fryns J-P (1991). X-linked mental retardation with marfanoid habitus (letter to editor). Am J Med Genet 38:233.
-
(1991)
Am J Med Genet
, vol.38
, pp. 233
-
-
Fryns, J.-P.1
-
10
-
-
0023470783
-
X-linked mental retardation with Marfanoid habitus
-
Fryns J-P, Buttiens M (1987). X-linked mental retardation with Marfanoid habitus. Am J Med Genet 28:267-274.
-
(1987)
Am J Med Genet
, vol.28
, pp. 267-274
-
-
Fryns, J.-P.1
Buttiens, M.2
-
11
-
-
0026357015
-
X-linked mental retardation with Marfanoid habitus: A changing phenotype with age?
-
Fryns J-P, Van Den Berghe H (1991). X-linked mental retardation with Marfanoid habitus: a changing phenotype with age? Genet Counsell 2:241-244.
-
(1991)
Genet Counsell
, vol.2
, pp. 241-244
-
-
Fryns, J.-P.1
Van Den Berghe, H.2
-
13
-
-
0026088569
-
A girl with the Lujan-Fryns syndrome
-
Gurrieri F, Neri G (1991). A girl with the Lujan-Fryns syndrome (letter to the editor). Am J Med Genet 38:290-291.
-
(1991)
Am J Med Genet
, vol.38
, pp. 290-291
-
-
Gurrieri, F.1
Neri, G.2
-
15
-
-
0036270836
-
The phenotypic consequences of MeCP2 mutations extend beyond Rett syndrome
-
Hammer S, Dorrani N, Dragich J, Kudo S, Schanen C (2002). The phenotypic consequences of MeCP2 mutations extend beyond Rett syndrome. Mental Retard Dev Disord Res Rev 8:94-98.
-
(2002)
Mental Retard Dev Disord Res Rev
, vol.8
, pp. 94-98
-
-
Hammer, S.1
Dorrani, N.2
Dragich, J.3
Kudo, S.4
Schanen, C.5
-
16
-
-
0033400911
-
Pseudoautosomal gene: Possible association with bipolar males but not with schizophrenia
-
Hawi Z, Mynett-Johnson L, Gill M, Murphy V, Straubl RE, Kendler KS, et al. (1999). Pseudoautosomal gene: possible association with bipolar males but not with schizophrenia. Psychiatr Genet 9:129-134.
-
(1999)
Psychiatr Genet
, vol.9
, pp. 129-134
-
-
Hawi, Z.1
Mynett-Johnson, L.2
Gill, M.3
Murphy, V.4
Straubl, R.E.5
Kendler, K.S.6
-
17
-
-
0034640699
-
Association between attention deficit hyperactivity disorder and the DXS7 locus
-
Jiang S, Xin R, Wu X, Lin S, Qian Y, Ren D, et al. (2000). Association between attention deficit hyperactivity disorder and the DXS7 locus. Am J Med Genet 96:289-292.
-
(2000)
Am J Med Genet
, vol.96
, pp. 289-292
-
-
Jiang, S.1
Xin, R.2
Wu, X.3
Lin, S.4
Qian, Y.5
Ren, D.6
-
19
-
-
0028559999
-
The Marfan syndrome gene locus as a favoured locus for susceptibility to schizophrenia
-
Kalsi G, Mankoo BS, Brynjolfsson J, Curtis D, Read T, Murphy P, et al. (1994). The Marfan syndrome gene locus as a favoured locus for susceptibility to schizophrenia. Psychiatr Genet 4:219-227.
-
(1994)
Psychiatr Genet
, vol.4
, pp. 219-227
-
-
Kalsi, G.1
Mankoo, B.S.2
Brynjolfsson, J.3
Curtis, D.4
Read, T.5
Murphy, P.6
-
20
-
-
0027488927
-
Lujan-Fryns syndrome (X linked mental retardation with Marfanoid habitus): Report of three cases and review
-
Lacombe D, Bonneau D, Verloes A, Couet D, Koulischer L, Battin J (1993). Lujan-Fryns syndrome (X linked mental retardation with Marfanoid habitus): report of three cases and review. Genet Counsell 4:193-198.
-
(1993)
Genet Counsell
, vol.4
, pp. 193-198
-
-
Lacombe, D.1
Bonneau, D.2
Verloes, A.3
Couet, D.4
Koulischer, L.5
Battin, J.6
-
21
-
-
0026085383
-
X-linked mental retardation with Marfanoid habitus: First report of four Italian patients
-
Lalatta F, Livini E, Selicorni A, Briscioli V, Vita A, Lugo M (1991). X-linked mental retardation with Marfanoid habitus: first report of four Italian patients. Am J Med Genet 38:228-232.
-
(1991)
Am J Med Genet
, vol.38
, pp. 228-232
-
-
Lalatta, F.1
Livini, E.2
Selicorni, A.3
Briscioli, V.4
Vita, A.5
Lugo, M.6
-
22
-
-
0034920299
-
Autism genetic resource exchange consortium (2001). A genomewide screen for autism susceptibility loci
-
Liu J, Nyholt DR, Magnussen P, Parano E, Pavone P, Geschwind D, et al. (2001). Autism genetic resource exchange consortium (2001). A genomewide screen for autism susceptibility loci. Am J Hum Genet 69:327-340.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 327-340
-
-
Liu, J.1
Nyholt, D.R.2
Magnussen, P.3
Parano, E.4
Pavone, P.5
Geschwind, D.6
-
23
-
-
0021357699
-
A form of X-linked mental retardation with Marfanoid habitus
-
Lujan JE, Carlin ME, Lubs HA (1984). A form of X-linked mental retardation with Marfanoid habitus. Am J Med Genet 17:311-322.
-
(1984)
Am J Med Genet
, vol.17
, pp. 311-322
-
-
Lujan, J.E.1
Carlin, M.E.2
Lubs, H.A.3
-
24
-
-
0030847759
-
Severe mental retardation with Marfanoid habitus in a young Lebanese male-a diagnostic challenge
-
Megarbane A, Chammas C (1997). Severe mental retardation with Marfanoid habitus in a young Lebanese male-a diagnostic challenge. Genet Counsell 8:195-200.
-
(1997)
Genet Counsell
, vol.8
, pp. 195-200
-
-
Megarbane, A.1
Chammas, C.2
-
26
-
-
0029102771
-
Models of comorbidity for multifactorial disorders
-
Neale MC, Kendler KS (1995). Models of comorbidity for multifactorial disorders. Am J Hum Genet 57:935-953.
-
(1995)
Am J Hum Genet
, vol.57
, pp. 935-953
-
-
Neale, M.C.1
Kendler, K.S.2
-
28
-
-
37649026213
-
Genome screen and follow-up analysis for autistic disorder
-
Shao Y, Wolpert CM, Raiford KL, Menold MM, Donnelly SL, Ravan SA, et al. (2002). Genome screen and follow-up analysis for autistic disorder. Am J Med Genet 114:99-105.
-
(2002)
Am J Med Genet
, vol.114
, pp. 99-105
-
-
Shao, Y.1
Wolpert, C.M.2
Raiford, K.L.3
Menold, M.M.4
Donnelly, S.L.5
Ravan, S.A.6
-
30
-
-
0342511713
-
X-linked mental retardation with Marfanoid habitus: The eye-catching psychiatric disorders
-
Spaepen A, Hellemans H, Fryns J-P (1994). X-linked mental retardation with Marfanoid habitus: the eye-catching psychiatric disorders. Am J Med Genet 51:611.
-
(1994)
Am J Med Genet
, vol.51
, pp. 611
-
-
Spaepen, A.1
Hellemans, H.2
Fryns, J.-P.3
-
31
-
-
0041320945
-
Terminal deletion of chromosome 5 in a patient with phenotypical features of Lujan-Fryns syndrome
-
Stathopulu E, Mackie-Ogilvie C, Flinter FA (2003). Terminal deletion of chromosome 5 in a patient with phenotypical features of Lujan-Fryns syndrome. Am J Med Genet 119A:363-366.
-
(2003)
Am J Med Genet
, vol.119 A
, pp. 363-366
-
-
Stathopulu, E.1
Mackie-Ogilvie, C.2
Flinter, F.A.3
-
32
-
-
0030607902
-
Autism and genetics: High incidence of specific genetic syndromes in 21 adolescents and adults living in two residential homes in Belgium
-
Swillen A, Hellemans H, Steyaert J, Fryns J-P (1996). Autism and genetics: high incidence of specific genetic syndromes in 21 adolescents and adults living in two residential homes in Belgium. Am J Med Genet (Neuropsychol Genet) 67:315-316.
-
(1996)
Am J Med Genet (Neuropsychol Genet)
, vol.67
, pp. 315-316
-
-
Swillen, A.1
Hellemans, H.2
Steyaert, J.3
Fryns, J.-P.4
-
33
-
-
0035036978
-
The clinical phenotype in institutionalised adult males with X-linked mental retardation (XLMR)
-
Van Buggenhout GJ, Trommelen JC, Brunner HG, Hame BC, Fryns J-P (2001). The clinical phenotype in institutionalised adult males with X-linked mental retardation (XLMR). Ann Genet 44:47-55.
-
(2001)
Ann Genet
, vol.44
, pp. 47-55
-
-
Van Buggenhout, G.J.1
Trommelen, J.C.2
Brunner, H.G.3
Hame, B.C.4
Fryns, J.-P.5
-
34
-
-
0034615176
-
Searching for a locus for schizophrenia within chromosome Xp11
-
Wei J, Hemmings GP (2000). Searching for a locus for schizophrenia within chromosome Xp11. Am J Med Genet 96:4-7.
-
(2000)
Am J Med Genet
, vol.96
, pp. 4-7
-
-
Wei, J.1
Hemmings, G.P.2
|