-
2
-
-
0004235298
-
-
American Psychiatric Association (APA) 4th edn. APA, Washington, DC
-
American Psychiatric Association (APA) (1994) Diagnostic and Statistical Manual of Mental Disorders, 4th edn. APA, Washington, DC.
-
(1994)
Diagnostic and Statistical Manual of Mental Disorders
-
-
-
3
-
-
0035822267
-
Chromosomal aberrations, subtelomeric defects, and mental retardation
-
Baralle D. (2001) Chromosomal aberrations, subtelomeric defects, and mental retardation. The Lancet 358, 7-8.
-
(2001)
The Lancet
, vol.358
, pp. 7-8
-
-
Baralle, D.1
-
5
-
-
4744343033
-
Diagnostic yield of genetic evaluations in developmental delay/mental retardation
-
Curry C. J., Sandhu A., Frutos L. & Wells R. (1997a) Diagnostic yield of genetic evaluations in developmental delay/mental retardation. Clinical Research 44, 214-23.
-
(1997)
Clinical Research
, vol.44
, pp. 214-223
-
-
Curry, C.J.1
Sandhu, A.2
Frutos, L.3
Wells, R.4
-
6
-
-
0030862260
-
Evaluation of mental retardation: Recommendations of a consensus conferences
-
Curry C. J., Stevenson R. E., Aughton D., Byrne J., Carey J. C., Cassidy S., Cunniff C., Graham J. M. Jr, Jones M. C., Kaback M. M., Moeschler J., Schaefer G. B., Schwartz S., Tarleton J. & Opitz J. (1997b) Evaluation of mental retardation: recommendations of a consensus conferences. American Journal of Medical Genetics 72, 468-77.
-
(1997)
American Journal of Medical Genetics
, vol.72
, pp. 468-477
-
-
Curry, C.J.1
Stevenson, R.E.2
Aughton, D.3
Byrne, J.4
Carey, J.C.5
Cassidy, S.6
Cunniff, C.7
Graham Jr., J.M.8
Jones, M.C.9
Kaback, M.M.10
Moeschler, J.11
Schaefer, G.B.12
Schwartz, S.13
Tarleton, J.14
Opitz, J.15
-
8
-
-
0035083965
-
Submicroscopic subtelomeric 1qter deletions: A recognisable phenotype?
-
De Vries B. B. A., Knight S. J. L., Homfray T., Smithson S. F., Flint J. & Winter R. M. (2001) Submicroscopic subtelomeric 1qter deletions: a recognisable phenotype? Journal of Medical Genetics 38, 175-8.
-
(2001)
Journal of Medical Genetics
, vol.38
, pp. 175-178
-
-
De Vries, B.B.A.1
Knight, S.J.L.2
Homfray, T.3
Smithson, S.F.4
Flint, J.5
Winter, R.M.6
-
9
-
-
16944362509
-
Screening and diagnosis for the fragile X syndrome among the mentally retarded: An epidemiological and psychological survey
-
Collaborative Fragile X Study Group
-
De Vries B. B., van den Ouweland A. M., Mohkamsing S., Duivenvoorden H. J., Mol E., Gelsema K., van Rijn M., Halley D. J., Sandkuijl L. A., Oostra B. A., Tibben A. & Niermeijer M. F. (1997) Screening and diagnosis for the fragile X syndrome among the mentally retarded: an epidemiological and psychological survey. Collaborative Fragile X Study Group. American Journal of Human Genetics 61, 660-7.
-
(1997)
American Journal of Human Genetics
, vol.61
, pp. 660-667
-
-
De Vries, B.B.1
van den Ouweland, A.M.2
Mohkamsing, S.3
Duivenvoorden, H.J.4
Mol, E.5
Gelsema, K.6
van Rijn, M.7
Halley, D.J.8
Sandkuijl, L.A.9
Oostra, B.A.10
Tibben, A.11
Niermeijer, M.F.12
-
10
-
-
0030795894
-
Cryptic terminal rearrangement of chromosome 22q13.32 detected by FISH in two unrelated patients
-
Doheny K. F., McDermid H. E., Harum K., Thomas G. H. & Raymond G. V. (1997) Cryptic terminal rearrangement of chromosome 22q13.32 detected by FISH in two unrelated patients. Journal of Medical Genetics 34, 640-4.
-
(1997)
Journal of Medical Genetics
, vol.34
, pp. 640-644
-
-
Doheny, K.F.1
McDermid, H.E.2
Harum, K.3
Thomas, G.H.4
Raymond, G.V.5
-
11
-
-
0035544938
-
The Siena Experience on rare neurological diseases: Diagnosis, therapy and research model for investigations of central and peripheral nervous systems and muscle
-
Federico A. & Dotti M. T. (2001) The Siena Experience on rare neurological diseases: diagnosis, therapy and research model for investigations of central and peripheral nervous systems and muscle. Functional Neurology 116, 263-70.
-
(2001)
Functional Neurology
, vol.116
, pp. 263-270
-
-
Federico, A.1
Dotti, M.T.2
-
12
-
-
0028798545
-
The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation
-
Flint J., Wilke A. O. M., Buckle V. J., Winter R. M., Holland A. L. & McDermid H. E. (1995) The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation. Nature Genetics 9, 132-9.
-
(1995)
Nature Genetics
, vol.9
, pp. 132-139
-
-
Flint, J.1
Wilke, A.O.M.2
Buckle, V.J.3
Winter, R.M.4
Holland, A.L.5
McDermid, H.E.6
-
14
-
-
0033552496
-
Defining the chromosomal basis of mental handicap
-
Hamerton J. L. & Stranc L. (1999) Defining the chromosomal basis of mental handicap. The Lancet 354, 1659-60.
-
(1999)
The Lancet
, vol.354
, pp. 1659-1660
-
-
Hamerton, J.L.1
Stranc, L.2
-
16
-
-
0033986825
-
Outcome of the routine assessment of patients with mental retardation in a genetics clinic
-
Hunter Alasdair G. W. (2000) Outcome of the routine assessment of patients with mental retardation in a genetics clinic. American Journal of Medical Genetics 90, 60-8.
-
(2000)
American Journal of Medical Genetics
, vol.90
, pp. 60-68
-
-
Hunter Alasdair, G.W.1
-
17
-
-
0003210740
-
Minor anomalies as clues to more serious problems and toward the recognition of malformation syndromes
-
5th edn, W.B. Saunders, Philadelphia
-
Jones K. L. (1997) Minor anomalies as clues to more serious problems and toward the recognition of malformation syndromes. In: Smith's Recognizable Patterns of Human Malformation 5th edn, pp. 727-46. W.B. Saunders, Philadelphia.
-
(1997)
Smith's Recognizable Patterns of Human Malformation
, pp. 727-746
-
-
Jones, K.L.1
-
18
-
-
0023476554
-
The prevalence of mental retardation
-
Kiely M. (1987) The prevalence of mental retardation. Epidemiological Reviews 9, 194-218.
-
(1987)
Epidemiological Reviews
, vol.9
, pp. 194-218
-
-
Kiely, M.1
-
19
-
-
0033552424
-
Subtle chromosomal rearrangements in children with unexplained mental retardation
-
Knight S., Regan R. & Nicod A. (1999) Subtle chromosomal rearrangements in children with unexplained mental retardation. The Lancet 354, 1676-81.
-
(1999)
The Lancet
, vol.354
, pp. 1676-1681
-
-
Knight, S.1
Regan, R.2
Nicod, A.3
-
20
-
-
0034018139
-
Correlations between socioeconomic status, level of IQ and aetiology in mental retardation: A population-based study of Norwegian children
-
Magnus P. (2000) Correlations between socioeconomic status, level of IQ and aetiology in mental retardation: a population-based study of Norwegian children. Social Psychiatry and Psychiatric Epidemiology 35, 12-8.
-
(2000)
Social Psychiatry and Psychiatric Epidemiology
, vol.35
, pp. 12-18
-
-
Magnus, P.1
-
21
-
-
0028952942
-
A population-based study of mild and severe mental retardation
-
Matilainen R., Airaksinen E., Mononen T., Launiala K. & Kaariainen R. (1995) A population-based study of mild and severe mental retardation. Acta Pediatrica 84, 261-6.
-
(1995)
Acta Pediatrica
, vol.84
, pp. 261-266
-
-
Matilainen, R.1
Airaksinen, E.2
Mononen, T.3
Launiala, K.4
Kaariainen, R.5
-
23
-
-
0034194867
-
Genes on the X Chromosome are important in undiagnosed mental retardation
-
Partington M., Mowat D., Einfeld S., Tonge B. & Turner G. (2000) Genes on the X Chromosome are important in undiagnosed mental retardation. American Journal of Medical Genetics 92, 57-1.
-
(2000)
American Journal of Medical Genetics
, vol.92
, pp. 57-61
-
-
Partington, M.1
Mowat, D.2
Einfeld, S.3
Tonge, B.4
Turner, G.5
-
28
-
-
0033629875
-
New insights into the genetic basis of intellectual disabilities
-
Skellern C., Lennox N. & Glasa I. (2000) New insights into the genetic basis of intellectual disabilities. Australian Family Physician 29, 41-5.
-
(2000)
Australian Family Physician
, vol.29
, pp. 41-45
-
-
Skellern, C.1
Lennox, N.2
Glasa, I.3
-
29
-
-
0034068232
-
Prevalence of psychiatric diagnoses in children with mental retardation: Data from a population-based study
-
Stromme P. & Diseth T. H. (2000) Prevalence of psychiatric diagnoses in children with mental retardation: data from a population-based study. Developmental Medicine and Child Neurology 42, 266-70.
-
(2000)
Developmental Medicine and Child Neurology
, vol.42
, pp. 266-270
-
-
Stromme, P.1
Diseth, T.H.2
-
30
-
-
0033950169
-
Aetiology in severe and mild mental retardation: A population-based study of Norwegian children
-
Stromme P. & Hagberg G. (2000) Aetiology in severe and mild mental retardation: a population-based study of Norwegian children. Developmental Medicine and Child Neurology 42, 76-86.
-
(2000)
Developmental Medicine and Child Neurology
, vol.42
, pp. 76-86
-
-
Stromme, P.1
Hagberg, G.2
-
33
-
-
0033016074
-
Aetiology of intellectual disability - The Finnish classification: Development of a method to incorporate WHO - 10 coding
-
Wilska M. & Kaski M. (1999) Aetiology of intellectual disability - the Finnish classification: development of a method to incorporate WHO - 10 coding. Journal of Intellectual Disabilitv Research 43, 242-50.
-
(1999)
Journal of Intellectual Disabilitv Research
, vol.43
, pp. 242-250
-
-
Wilska, M.1
Kaski, M.2
-
34
-
-
0030031950
-
What's in a face
-
Winter R. M. (1996) What's in a face. Nature Genetics 12, 124-9.
-
(1996)
Nature Genetics
, vol.12
, pp. 124-129
-
-
Winter, R.M.1
|