-
1
-
-
0030061403
-
The Nisonger CBRF: A child behaviour rating form for children with developmental disabilities
-
AMAN M., TASSE M., ROJAHN J., HAMMER D.: The Nisonger CBRF: a child behaviour rating form for children with developmental disabilities. Res. Dev. Disabil., 1996, 17, 41-57.
-
(1996)
Res. Dev. Disabil.
, vol.17
, pp. 41-57
-
-
Aman, M.1
Tasse, M.2
Rojahn, J.3
Hammer, D.4
-
2
-
-
0031715265
-
Development of the Children's Communication Checklist (CGC): A method for assessing qualitative aspects of communicative impairment in children
-
BISHOP D.: Development of the Children's Communication Checklist (CGC): a method for assessing qualitative aspects of communicative impairment in children. J. Child Psychol. Psychiatry, 1998, 39, 879-891.
-
(1998)
J. Child Psychol. Psychiatry
, vol.39
, pp. 879-891
-
-
Bishop, D.1
-
3
-
-
0035214135
-
Parent and teacher report of pragmatic aspects of communication : Use of the Children's Communication checklist in a clinical setting
-
BISHOP D., BAIRD G.: Parent and teacher report of pragmatic aspects of communication : use of the Children's Communication checklist in a clinical setting. Dev. Med. Child Neurol., 2001, 43, 809-818.
-
(2001)
Dev. Med. Child Neurol.
, vol.43
, pp. 809-818
-
-
Bishop, D.1
Baird, G.2
-
4
-
-
0032323563
-
Problem behaviours associated with deletion Prader-Willi, Smith-Magenis, and Cri du Chat syndromes
-
CLARKE D., BOER H.: Problem behaviours associated with deletion Prader-Willi, Smith-Magenis, and Cri du Chat syndromes. Am. J. Ment. Retard., 1998, 103, 264-271.
-
(1998)
Am. J. Ment. Retard.
, vol.103
, pp. 264-271
-
-
Clarke, D.1
Boer, H.2
-
5
-
-
0032457871
-
Distinctiveness and correlates of maladaptive behaviour in children and adolescents with Smith-Magenis syndrome
-
DYKENS E., SMITH A.: Distinctiveness and correlates of maladaptive behaviour in children and adolescents with Smith-Magenis syndrome. J. Intell. Disabilit. Res., 1998, 42, 481-489.
-
(1998)
J. Intell. Disabilit. Res.
, vol.42
, pp. 481-489
-
-
Dykens, E.1
Smith, A.2
-
6
-
-
0031115936
-
Brief report: Cognitive and behavioural profiles in persons with Smith-Magenis syndrome
-
DYKENS E., FINUCANE B., GAYLEY C.: Brief report: cognitive and behavioural profiles in persons with Smith-Magenis syndrome. J. Autism Dev. Disord., 1997, 27, 203-211.
-
(1997)
J. Autism Dev. Disord.
, vol.27
, pp. 203-211
-
-
Dykens, E.1
Finucane, B.2
Gayley, C.3
-
7
-
-
0035114739
-
Characterization of self-injurious behaviors in children and adults with Smith-Magenis syndrome
-
FINUCANE B., DIRRIGL K., SIMON E.: Characterization of self-injurious behaviors in children and adults with Smith-Magenis syndrome. Am. J. Ment. Retard., 2001, 106, 52-58.
-
(2001)
Am. J. Ment. Retard.
, vol.106
, pp. 52-58
-
-
Finucane, B.1
Dirrigl, K.2
Simon, E.3
-
8
-
-
0026347929
-
Molecular analysis of the Smith-Magenis syndrome: A possible contiguous-gene syndrome associated with del(17) (p11.2)
-
GREENBERG F., GUZETTA V., DE OCA-LUNA R., MAGENIS R., SMITH A., RICHTER S., KONDO I., DOBYNS W., PATEL P., LUPSKI J.: Molecular analysis of the Smith-Magenis syndrome: A possible contiguous-gene syndrome associated with del(17) (p11.2). Am. J. Med. Genet., 1991, 4, 1207-1218.
-
(1991)
Am. J. Med. Genet.
, vol.4
, pp. 1207-1218
-
-
Greenberg, F.1
Guzetta, V.2
De Oca-Luna, R.3
Magenis, R.4
Smith, A.5
Richter, S.6
Kondo, I.7
Dobyns, W.8
Patel, P.9
Lupski, J.10
-
9
-
-
0029920807
-
Multidisciplinary clinical study of Smith-Magenis syndrome: (deletion 17p11.2)
-
GREENBERG F., LEWIS R., POTOCKI L., GLAZE D., PARKE J., KILLIAN J., MURPHA M., WILLIAMSON D., BROWN F., DUTTON R., MCCLUGGAGE C., FRIEDMAN S., SULEK M., LUPSKI J.: Multidisciplinary clinical study of Smith-Magenis syndrome: (deletion 17p11.2). Am. J. Med. Genet., 1996, 62, 247-254.
-
(1996)
Am. J. Med. Genet.
, vol.62
, pp. 247-254
-
-
Greenberg, F.1
Lewis, R.2
Potocki, L.3
Glaze, D.4
Parke, J.5
Killian, J.6
Murpha, M.7
Williamson, D.8
Brown, F.9
Dutton, R.10
Mccluggage, C.11
Friedman, S.12
Sulek, M.13
Lupski, J.14
-
10
-
-
4844221272
-
-
Heidelberg, Edition Schindele
-
HOLTZ K., EBERLE G., HILLIG A., MARKER K.: HKI - Heidelberger Kompetenz Inventar für geistig Behinderte. Heidelberg, Edition Schindele, 1998.
-
(1998)
HKI - Heidelberger Kompetenz Inventar für Geistig Behinderte
-
-
Holtz, K.1
Eberle, G.2
Hillig, A.3
Marker, K.4
-
11
-
-
0031765717
-
Stress and coping in families with children with Smith-Magenis syndrome
-
HODAPP R., FIDLER D., SMITH A.: Stress and coping in families with children with Smith-Magenis syndrome. J. Intell. Disabil. Res., 1998, 42, 331-340.
-
(1998)
J. Intell. Disabil. Res.
, vol.42
, pp. 331-340
-
-
Hodapp, R.1
Fidler, D.2
Smith, A.3
-
12
-
-
0022543280
-
Interstitial deletion of (17) (p11.2p11.2) in nine patients
-
SMITH A., MCGAVRAN L., ROBINSON J., WALDSTEIN G., MACFARLANE J., ZONONA J., REISS J., LAHR M., ALLEN L., MAGENIS E.: Interstitial deletion of (17) (p11.2p11.2) in nine patients. Am. J. Med. Genet., 1986, 24, 393-414.
-
(1986)
Am. J. Med. Genet.
, vol.24
, pp. 393-414
-
-
Smith, A.1
Mcgavran, L.2
Robinson, J.3
Waldstein, G.4
Macfarlane, J.5
Zonona, J.6
Reiss, J.7
Lahr, M.8
Allen, L.9
Magenis, E.10
-
13
-
-
0030065597
-
The Nisonger Child Behavior Rating Form: Age and gender effects and norms
-
TASSE M., AMAN M., HAMMER D., ROJAHN J.: The Nisonger Child Behavior Rating Form : age and gender effects and norms. Res. Dev. Disabil., 1996, 17, 59-75.
-
(1996)
Res. Dev. Disabil.
, vol.17
, pp. 59-75
-
-
Tasse, M.1
Aman, M.2
Hammer, D.3
Rojahn, J.4
-
14
-
-
0035207224
-
Abilities and attainment in Smith-Magenis syndrome
-
UDWIN O., WEBBER C., HORN I.: Abilities and attainment in Smith-Magenis syndrome. Dev. Med. Child Neurol., 2001, 43, 823-828.
-
(2001)
Dev. Med. Child Neurol.
, vol.43
, pp. 823-828
-
-
Udwin, O.1
Webber, C.2
Horn, I.3
-
15
-
-
0034086132
-
Three young children with Smith-Magenis syndrome: Their distinct, recognisable behavioural phenotype as the most important clinical symptoms
-
WILLEKENS D., DECOCK P., FRYNS J.: Three young children with Smith-Magenis syndrome: Their distinct, recognisable behavioural phenotype as the most important clinical symptoms. Genet. Counsel., 2000, 11, 103-110.
-
(2000)
Genet. Counsel.
, vol.11
, pp. 103-110
-
-
Willekens, D.1
Decock, P.2
Fryns, J.3
|