-
2
-
-
0035464960
-
Monogenic causes of X-linked mental retardation
-
Chelly J. & Mandel J. (2001) Monogenic causes of X-linked mental retardation. Nature Reviews Genetics 2, 669-80.
-
(2001)
Nature Reviews Genetics
, vol.2
, pp. 669-680
-
-
Chelly, J.1
Mandel, J.2
-
4
-
-
4444236954
-
Annotation: Deconstructing the attention deficit in fragile X syndrome: A developmental neuropsychological approach
-
Cornish K. M., Turk J., Wilding J., Sudhalter V., Munir F., Kooy F. & Hagerman R. (2004) Annotation: Deconstructing the attention deficit in fragile X syndrome: A developmental neuropsychological approach. Journal of Child Psychology and Psychiatry 45, 1042-53.
-
(2004)
Journal of Child Psychology and Psychiatry
, vol.45
, pp. 1042-1053
-
-
Cornish, K.M.1
Turk, J.2
Wilding, J.3
Sudhalter, V.4
Munir, F.5
Kooy, F.6
Hagerman, R.7
-
6
-
-
0036948994
-
X-linked mental retardation: Vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms
-
Frints S. G. M., Froyen G., Marynen P. & Fryns J. P. (2002) X-linked mental retardation: Vanishing boundaries between non-specific (MRX) and syndromic (MRXS) forms. Clinical Genetics 62, 423-32.
-
(2002)
Clinical Genetics
, vol.62
, pp. 423-432
-
-
Frints, S.G.M.1
Froyen, G.2
Marynen, P.3
Fryns, J.P.4
-
8
-
-
33746441990
-
Prader-Willi and Angelman syndromes: From childhood to adult life
-
In (eds P. Howlin & O. Udwin), Cambridge University Press, Cambridge, UK
-
Holland A., Whittington J. & Butler J. (2002) Prader-Willi and Angelman syndromes: From childhood to adult life. In: Outcomes in Neurodevelopmental and Genetic Disorders (eds P. Howlin & O. Udwin), pp. 220-40. Cambridge University Press, Cambridge, UK.
-
(2002)
Outcomes in Neurodevelopmental and Genetic Disorders
, pp. 220-240
-
-
Holland, A.1
Whittington, J.2
Butler, J.3
-
9
-
-
2342535716
-
Zinc finger 81 (ZNF81) mutations associated with X-linked mental retardation
-
Kleefstra T., Yntema H. G., Oudakker A. R., Banning M. J., Kalsheuer V. M., Chelly J., Moraine C., Ropers H. H., Fryns J. P., Janssen I. M., Sistermans E. A., Nillesen W. N., de Vries L. B., Hamel B. C. & van Bokhoven H. (2004) Zinc finger 81 (ZNF81) mutations associated with X-linked mental retardation. Journal of Medical Genetics 41, 394-9.
-
(2004)
Journal of Medical Genetics
, vol.41
, pp. 394-399
-
-
Kleefstra, T.1
Yntema, H.G.2
Oudakker, A.R.3
Banning, M.J.4
Kalsheuer, V.M.5
Chelly, J.6
Moraine, C.7
Ropers, H.H.8
Fryns, J.P.9
Janssen, I.M.10
Sistermans, E.A.11
Nillesen, W.N.12
de Vries, L.B.13
Hamel, B.C.14
van Bokhoven, H.15
-
10
-
-
0035293377
-
Noncompaction of the myocardium associated with Roifman syndrome
-
Mandel K., Grunebaum E. & Benson L. (2001) Noncompaction of the myocardium associated with Roifman syndrome. Cardiology in the Young 11, 240-3.
-
(2001)
Cardiology in the Young
, vol.11
, pp. 240-243
-
-
Mandel, K.1
Grunebaum, E.2
Benson, L.3
-
12
-
-
0000258901
-
Le test de copie d'une figure complexe
-
Translated by Corwyn J. & Bylsma F. W. (1993) with commentary. Clinical Psychologist 7, 9-15
-
Osterrieth P. A. (1944) Le test de copie d'une figure complexe. Archives de Psychologie 30, 206-356. Translated by Corwyn J. & Bylsma F. W. (1993) with commentary. Clinical Psychologist 7, 9-15.
-
(1944)
Archives De Psychologie
, vol.30
, pp. 206-356
-
-
Osterrieth, P.A.1
-
13
-
-
0034082145
-
Hypogonadotrophic hypogonadism in Roifman syndrome
-
Robertson S. P., Rodda C. & Bankier A. (2000) Hypogonadotrophic hypogonadism in Roifman syndrome. Clinical Genetics 57, 435-8.
-
(2000)
Clinical Genetics
, vol.57
, pp. 435-438
-
-
Robertson, S.P.1
Rodda, C.2
Bankier, A.3
-
14
-
-
0032984058
-
Antibody deficiency, growth retardation, spondyloepiphyseal dysplasia and retinal dystrophy: A novel syndrome
-
Roifman C. M. (1999) Antibody deficiency, growth retardation, spondyloepiphyseal dysplasia and retinal dystrophy: A novel syndrome. Clinical Genetics 55, 103-9.
-
(1999)
Clinical Genetics
, vol.55
, pp. 103-109
-
-
Roifman, C.M.1
-
15
-
-
3843100409
-
Williams and Smith-Magenis syndromes
-
In: (eds P. Howlin & O. Udwin), Cambridge University Press, Cambridge, UK
-
Udwin O. (2002) Williams and Smith-Magenis syndromes. In: Outcomes in Neurodevelopmental and Genetic Disorders (eds P. Howlin & O. Udwin), pp. 299-325. Cambridge University Press, Cambridge, UK.
-
(2002)
Outcomes in Neurodevelopmental and Genetic Disorders
, pp. 299-325
-
-
Udwin, O.1
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