-
1
-
-
0015227656
-
From gene to behavior
-
Benzer S. From gene to behavior. JAMA 1971; 18: 1015-22.
-
(1971)
JAMA
, vol.18
, pp. 1015-1022
-
-
Benzer, S.1
-
2
-
-
0015861503
-
The genetics of behavior
-
Brenner S. The genetics of behavior. Br Med Bull 1973; 29: 269-71.
-
(1973)
Br Med Bull
, vol.29
, pp. 269-271
-
-
Brenner, S.1
-
4
-
-
0026783363
-
Chromosomal aberrations and schizophrenia: Autosomes
-
Bassett AS. Chromosomal aberrations and schizophrenia: autosomes. Br J Psychiatry 1992; 161: 323-34.
-
(1992)
Br J Psychiatry
, vol.161
, pp. 323-334
-
-
Bassett, A.S.1
-
6
-
-
0028100408
-
Psychiatric genetics: Research challenges and pathways forward
-
Rutter M. Psychiatric genetics: research challenges and pathways forward. Am J Med Genet 1994; 54: 185-98.
-
(1994)
Am J Med Genet
, vol.54
, pp. 185-198
-
-
Rutter, M.1
-
7
-
-
0004235298
-
-
Washington, DC: American Psychiatric Association, 1987
-
American Psychiatric Association. Diagnostic and statistical manual of mental disorders. 3rd ed, revised 3rd ed, and 4th ed. Washington, DC: American Psychiatric Association, 1980, 1987, 1994.
-
(1980)
Diagnostic and Statistical Manual of Mental Disorders. 3rd Ed, Revised 3rd Ed, and 4th Ed.
-
-
-
8
-
-
0013663724
-
Chromosome preparations of leukocytes cultured from human peripheral blood
-
Moorhead PS, Nowell PC, Mellnan WJ, Battips DM, Hungford DA. Chromosome preparations of leukocytes cultured from human peripheral blood. Exp Cell Res 1960; 20: 613-6.
-
(1960)
Exp Cell Res
, vol.20
, pp. 613-616
-
-
Moorhead, P.S.1
Nowell, P.C.2
Mellnan, W.J.3
Battips, D.M.4
Hungford, D.A.5
-
10
-
-
0025304617
-
The common fragile site in band q27 of the human X chromosome is not coincident with the fragile X
-
Sutherland GR, Baker E. The common fragile site in band q27 of the human X chromosome is not coincident with the fragile X. Clin Genet 1990; 37: 167-72.
-
(1990)
Clin Genet
, vol.37
, pp. 167-172
-
-
Sutherland, G.R.1
Baker, E.2
-
11
-
-
0016790765
-
Standardization in human cytogenetics
-
Paris conference supplement. Standardization in human cytogenetics. Cytogenet Cell Genet 1975; 18: 201-38.
-
(1975)
Cytogenet Cell Genet
, vol.18
, pp. 201-238
-
-
-
12
-
-
84908766874
-
An international system for human cytogenetic nomenclature: High resolution banding
-
1981
-
ISCN. An international system for human cytogenetic nomenclature: high resolution banding. Birth Defects Original Article Series XVII, 1978, 1981, 1985.
-
(1978)
Birth Defects Original Article Series XVII
-
-
-
15
-
-
0002418993
-
The frequency of chromosomal abnormalities detected in consecutive new-born studies
-
Hook EB, Porter IH, eds. New York: Academic Press
-
Hook EB, Hamerton JL. The frequency of chromosomal abnormalities detected in consecutive new-born studies. In: Hook EB, Porter IH, eds. Population cytogenetics. New York: Academic Press, 1977: 63-79.
-
(1977)
Population Cytogenetics
, pp. 63-79
-
-
Hook, E.B.1
Hamerton, J.L.2
-
16
-
-
0025032986
-
Review: The role of chromosome abnormalities in reproductive failure
-
Jacobs PA. Review: the role of chromosome abnormalities in reproductive failure. Reprod Nutr Dev Suppl 1990; 1: 63-74.
-
(1990)
Reprod Nutr Dev Suppl
, vol.1
, pp. 63-74
-
-
Jacobs, P.A.1
-
17
-
-
0024987918
-
A clinical and cytogenetic study of institutionalized mental retardates
-
Kumada T. A clinical and cytogenetic study of institutionalized mental retardates. Hiroshima J Med Sci 1990; 39: 39-56.
-
(1990)
Hiroshima J Med Sci
, vol.39
, pp. 39-56
-
-
Kumada, T.1
-
18
-
-
0018934468
-
Chromosome variants in children referred for cytogenetic examination from two paediatric departments during a 12-year period
-
Krag-Olsen B, Nielsen J, Dirdal M, Holm V, Haahr J, Rasmussen NH, Videbech P, Yanagisawa S. Chromosome variants in children referred for cytogenetic examination from two paediatric departments during a 12-year period. Hum Genet 1980; 56: 67-9.
-
(1980)
Hum Genet
, vol.56
, pp. 67-69
-
-
Krag-Olsen, B.1
Nielsen, J.2
Dirdal, M.3
Holm, V.4
Haahr, J.5
Rasmussen, N.H.6
Videbech, P.7
Yanagisawa, S.8
-
19
-
-
0017517247
-
Cytogenetic study of individuals suspected of chromosome anomalies
-
Singh DN. Cytogenetic study of individuals suspected of chromosome anomalies. Clin Pediatr 1977; 16: 619-22.
-
(1977)
Clin Pediatr
, vol.16
, pp. 619-622
-
-
Singh, D.N.1
-
20
-
-
0018838859
-
Incidence of major chromosomal abnormalities in a referred population for suspected chromosomal aberrations: A report of 357 cases
-
Verma RS, Dosik H. Incidence of major chromosomal abnormalities in a referred population for suspected chromosomal aberrations: a report of 357 cases. Clin Genet 1980; 17: 305-8.
-
(1980)
Clin Genet
, vol.17
, pp. 305-308
-
-
Verma, R.S.1
Dosik, H.2
-
21
-
-
0015258196
-
Chromosome findings in 700 children referred to a psychiatric clinic
-
Crandall BF, Carrel RE, Sparkes RS. Chromosome findings in 700 children referred to a psychiatric clinic. J Pediatr 1972; 80: 62-8.
-
(1972)
J Pediatr
, vol.80
, pp. 62-68
-
-
Crandall, B.F.1
Carrel, R.E.2
Sparkes, R.S.3
-
22
-
-
0029197021
-
Cytogenetic studies in clinical diagnosis - Analysis of 1611 examination results
-
Bocian E, Mazurczak T, Stanczak H. Cytogenetic studies in clinical diagnosis - analysis of 1611 examination results. Przegl Lek 1995; 52: 5-9.
-
(1995)
Przegl Lek
, vol.52
, pp. 5-9
-
-
Bocian, E.1
Mazurczak, T.2
Stanczak, H.3
-
23
-
-
0038102354
-
Chromosomal abnormalities
-
Rutter M, Taylor E, Hersov L, eds. Oxford: Blackwell Scientific Publication
-
Bolton P, Holland A. Chromosomal abnormalities. In: Rutter M, Taylor E, Hersov L, eds. Child and adolescent psychiatry. 3rd ed. Oxford: Blackwell Scientific Publication, 1994: 152-71.
-
(1994)
Child and Adolescent Psychiatry. 3rd Ed.
, pp. 152-171
-
-
Bolton, P.1
Holland, A.2
-
24
-
-
0025245438
-
The UCLA-University of Utah epidemiologic survey of autism: The etiologic role of rare diseases
-
Ritvo ER, Mason-Brothers A, Freeman BJ, Pingree C, Jensen WR, McMahon WM, Petersen PB, Jorde LB, Mo A, Ritvo A. The UCLA-University of Utah epidemiologic survey of autism: the etiologic role of rare diseases. Am J Psychiatry 1990; 147: 1614-21.
-
(1990)
Am J Psychiatry
, vol.147
, pp. 1614-1621
-
-
Ritvo, E.R.1
Mason-Brothers, A.2
Freeman, B.J.3
Pingree, C.4
Jensen, W.R.5
McMahon, W.M.6
Petersen, P.B.7
Jorde, L.B.8
Mo, A.9
Ritvo, A.10
-
26
-
-
0029037095
-
The awareness of chromosomal disarrangements in the evaluation of child psychiatry patients
-
Levy PA, Dalton R, Shapira E. The awareness of chromosomal disarrangements in the evaluation of child psychiatry patients. Child Psychiatry Hum Dev 1995; 25: 281-7.
-
(1995)
Child Psychiatry Hum Dev
, vol.25
, pp. 281-287
-
-
Levy, P.A.1
Dalton, R.2
Shapira, E.3
-
29
-
-
10644252651
-
The developing brain and mind: Advances in research techniques
-
Lewis M, ed. Baltimore: Williams & Wilkins
-
Young JG, Brasic JR, Ostre H, Kaplan D, Will M, John ER, Prichep L, Buchsaum M. The developing brain and mind: advances in research techniques. In: Child and adolescent psychiatry. 2nd ed, Lewis M, ed. Baltimore: Williams & Wilkins, 1996: 1209-34.
-
(1996)
Child and Adolescent Psychiatry. 2nd Ed
, pp. 1209-1234
-
-
Young, J.G.1
Brasic, J.R.2
Ostre, H.3
Kaplan, D.4
Will, M.5
John, E.R.6
Prichep, L.7
Buchsaum, M.8
-
30
-
-
0018389885
-
Pericentric inversions of chromosome number 9: Benign or harmful?
-
Howard-Peebles PN, Stoddard GR. Pericentric inversions of chromosome number 9: benign or harmful? Hum Hered 1979; 29: 111-7.
-
(1979)
Hum Hered
, vol.29
, pp. 111-117
-
-
Howard-Peebles, P.N.1
Stoddard, G.R.2
-
31
-
-
0021710068
-
Pericentric inversions: Problems and significance for clinical genetics
-
Kaiser P. Pericentric inversions: problems and significance for clinical genetics. Human Genet 1984; 69: 1-47.
-
(1984)
Human Genet
, vol.69
, pp. 1-47
-
-
Kaiser, P.1
-
32
-
-
0026827955
-
Correlation of the clinical phenotype with a pericentric inversion of chromosome 9
-
Scarínci R, Anichini C, Vivarelli R, Berardi R, Pucci L, Rosaia L, Tomaccini D. Correlation of the clinical phenotype with a pericentric inversion of chromosome 9. Boll Soc Ital Biol Sper 1992; 68: 175-81.
-
(1992)
Boll Soc Ital Biol Sper
, vol.68
, pp. 175-181
-
-
Scarínci, R.1
Anichini, C.2
Vivarelli, R.3
Berardi, R.4
Pucci, L.5
Rosaia, L.6
Tomaccini, D.7
-
33
-
-
0024448026
-
Pericentric inversion chromosome 9 and personality disorder
-
Kumar HV. Pericentric inversion chromosome 9 and personality disorder. Br J Psychiatry 1989; 155: 408-10.
-
(1989)
Br J Psychiatry
, vol.155
, pp. 408-410
-
-
Kumar, H.V.1
-
34
-
-
0027208102
-
Pericentric region of chromosome 9 is a possible candidate region for linkage study of schizophrenia
-
Nanko S, Kunugi H, Sasaki T, Fukuda R, Kawate T, Kazamatsuri H. Pericentric region of chromosome 9 is a possible candidate region for linkage study of schizophrenia. Biol Psychiatry 1993; 33: 655-8.
-
(1993)
Biol Psychiatry
, vol.33
, pp. 655-658
-
-
Nanko, S.1
Kunugi, H.2
Sasaki, T.3
Fukuda, R.4
Kawate, T.5
Kazamatsuri, H.6
-
35
-
-
0027210744
-
Schizophrenia with pericentric inversion of chromosome 9: A case report
-
Nanko S. Schizophrenia with pericentric inversion of chromosome 9: a case report. Jpn J Psychiatry Neurol 1993; 47: 47-9.
-
(1993)
Jpn J Psychiatry Neurol
, vol.47
, pp. 47-49
-
-
Nanko, S.1
-
36
-
-
0018294645
-
Chromosomal variants in mentally retarded and normal men
-
Soudek D, Sroka H. Chromosomal variants in mentally retarded and normal men. Clin Genet 1979; 16: 109-16.
-
(1979)
Clin Genet
, vol.16
, pp. 109-116
-
-
Soudek, D.1
Sroka, H.2
-
37
-
-
0025579568
-
Pericentric inversion of chromosome 9: Prevalence in 300 Down syndrome families and molecular studies of nondisjunction
-
Serra A, Brahe C, Millington-Ward A, Neri G, Tedeschi B, Tassone F, Bova R. Pericentric inversion of chromosome 9: prevalence in 300 Down syndrome families and molecular studies of nondisjunction. Am J Med Genet Suppl 1990; 7: 162-8.
-
(1990)
Am J Med Genet Suppl
, vol.7
, pp. 162-168
-
-
Serra, A.1
Brahe, C.2
Millington-Ward, A.3
Neri, G.4
Tedeschi, B.5
Tassone, F.6
Bova, R.7
-
38
-
-
0023232927
-
Chromosomal polymorphisms of 1, 9, 16 and Y in 4 major ethnic groups: A large prenatal study
-
Hsu LYF, Benn PA, Tannenbaum HL, Perils TE, Carlson AD. Chromosomal polymorphisms of 1, 9, 16 and Y in 4 major ethnic groups: a large prenatal study. Am J Med Genet 1987; 26: 95-101.
-
(1987)
Am J Med Genet
, vol.26
, pp. 95-101
-
-
Hsu, L.Y.F.1
Benn, P.A.2
Tannenbaum, H.L.3
Perils, T.E.4
Carlson, A.D.5
-
39
-
-
0026850391
-
Pericentric inversions of chromosome 9 in Taiwanese fetuses
-
Ko TM, Hsieh FJ, Chang LS, Pan MF, Lee TY. Pericentric inversions of chromosome 9 in Taiwanese fetuses. J Formos Med Assoc 1992; 91: 473-4.
-
(1992)
J Formos Med Assoc
, vol.91
, pp. 473-474
-
-
Ko, T.M.1
Hsieh, F.J.2
Chang, L.S.3
Pan, M.F.4
Lee, T.Y.5
-
40
-
-
0027073145
-
Population studies of INV (9) chromosomes in 4,300 Japanese: Incidence, sex difference and clinical significance
-
Yamada K. Population studies of INV (9) chromosomes in 4,300 Japanese: incidence, sex difference and clinical significance. Jpn J Hum Genet 1992; 37: 293-301.
-
(1992)
Jpn J Hum Genet
, vol.37
, pp. 293-301
-
-
Yamada, K.1
-
41
-
-
0029917626
-
Cytogenetic and epidemiological findings in Down syndrome, England and Wales 1989 to 1993. National Down syndrome cytogenetic register and the association of clinical cytogeneticists
-
Mutton D, Alberman E, Hook EB. Cytogenetic and epidemiological findings in Down syndrome, England and Wales 1989 to 1993. National Down syndrome cytogenetic register and the association of clinical cytogeneticists. J Med Genet 1996; 33: 387-94.
-
(1996)
J Med Genet
, vol.33
, pp. 387-394
-
-
Mutton, D.1
Alberman, E.2
Hook, E.B.3
-
42
-
-
3643070127
-
Fragile X and other heritable fragile sites on human chromosomes
-
Barch MJ, ed. New York: Raven Press
-
Jacky P. Fragile X and other heritable fragile sites on human chromosomes. In: Barch MJ, ed. The ACT cytogentics laboratory manual. 2nd ed. New York: Raven Press, 1991: 489-523.
-
(1991)
The ACT Cytogentics Laboratory Manual. 2nd Ed.
, pp. 489-523
-
-
Jacky, P.1
-
43
-
-
0023099792
-
Fragile sites still a mystery
-
Jordan BR. Fragile sites still a mystery. Lancet 1987; i: 497-8.
-
(1987)
Lancet
, vol.1
, pp. 497-498
-
-
Jordan, B.R.1
-
44
-
-
0025905795
-
Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome
-
Verkerk AJMH, Pieretti M, Sutcliffe JS, Fu YH, Kuhl DP, Pizzuti A, Reiner O, Richards S, Victoria MF, Zhang F, Eussen BE, van Ommen GB, Blonden LAJ, Riggins GJ, Chastain JL, Kunst CB, Galjaard H, Caskey CT, Nelson DL, Oostra BA, Warren ST. Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome. Cell 1991; 65: 905-14.
-
(1991)
Cell
, vol.65
, pp. 905-914
-
-
Verkerk, A.J.M.H.1
Pieretti, M.2
Sutcliffe, J.S.3
Fu, Y.H.4
Kuhl, D.P.5
Pizzuti, A.6
Reiner, O.7
Richards, S.8
Victoria, M.F.9
Zhang, F.10
Eussen, B.E.11
Van Ommen, G.B.12
Blonden, L.A.J.13
Riggins, G.J.14
Chastain, J.L.15
Kunst, C.B.16
Galjaard, H.17
Caskey, C.T.18
Nelson, D.L.19
Oostra, B.A.20
Warren, S.T.21
more..
-
45
-
-
0028712179
-
Fragile X syndrome
-
Laxova R. Fragile X syndrome. Adv Pediatr 1994; 41: 305-42.
-
(1994)
Adv Pediatr
, vol.41
, pp. 305-342
-
-
Laxova, R.1
-
46
-
-
0027606381
-
Fragile site X chromosomes in mentally retarded boys
-
Moon HR, Moon SY. Fragile site X chromosomes in mentally retarded boys. J Korean Med Sci 1993; 8: 192-6.
-
(1993)
J Korean Med Sci
, vol.8
, pp. 192-196
-
-
Moon, H.R.1
Moon, S.Y.2
-
47
-
-
0023759213
-
A cytogenetic study of mentally retarded school children in Taiwan with special reference to the fragile X chromosome
-
Li SY, Tsai CC, Chou MY, Lin JK. A cytogenetic study of mentally retarded school children in Taiwan with special reference to the fragile X chromosome. Hum Genet 1988; 79: 292-6.
-
(1988)
Hum Genet
, vol.79
, pp. 292-296
-
-
Li, S.Y.1
Tsai, C.C.2
Chou, M.Y.3
Lin, J.K.4
-
48
-
-
0026641068
-
Fragile X positivity in Chinese children with autistic spectrum disorder
-
Wong VC, Lam ST. Fragile X positivity in Chinese children with autistic spectrum disorder. Pediatr Neurol 1992; 8: 272-4.
-
(1992)
Pediatr Neurol
, vol.8
, pp. 272-274
-
-
Wong, V.C.1
Lam, S.T.2
-
50
-
-
0023747113
-
The fragile X-chromosome: An evaluation of the results in a routine cytogenetic laboratory in the period 1981-1986
-
Veenema H, Beverstock GC, de Koning T, Pearson PL, van de Kamp JJ. The fragile X-chromosome: an evaluation of the results in a routine cytogenetic laboratory in the period 1981-1986. Clin Genet 1988; 33: 410-7.
-
(1988)
Clin Genet
, vol.33
, pp. 410-417
-
-
Veenema, H.1
Beverstock, G.C.2
De Koning, T.3
Pearson, P.L.4
Van De Kamp, J.J.5
-
52
-
-
0023945418
-
Fragile-X syndrome: A particular epileptogenic EEG pattern
-
Musumeci SA, Colognola RM, Ferri R, Gigli GL, Petrella MA, Sanfilippo S, Bergonzi P, Tassinari CA. Fragile-X syndrome: a particular epileptogenic EEG pattern. Epilepsia 1988; 29: 41-7.
-
(1988)
Epilepsia
, vol.29
, pp. 41-47
-
-
Musumeci, S.A.1
Colognola, R.M.2
Ferri, R.3
Gigli, G.L.4
Petrella, M.A.5
Sanfilippo, S.6
Bergonzi, P.7
Tassinari, C.A.8
-
53
-
-
0023925498
-
The EEG in early diagnosis of Angelman's (happy puppet) syndrome
-
Boyd SG, Harden A, Patton MA. The EEG in early diagnosis of Angelman's (happy puppet) syndrome. Eur J Pediatr 1988; 147: 503-13.
-
(1988)
Eur J Pediatr
, vol.147
, pp. 503-513
-
-
Boyd, S.G.1
Harden, A.2
Patton, M.A.3
-
54
-
-
0009875107
-
Laboratory and diagnostic testing
-
Wiener JM, ed. Washington, DC: American Psychiatric Press
-
Zametkin AJ, Andreason P, Krusei MJP. Laboratory and diagnostic testing. In: Textbook of child and adolescent psychiatry. 1st ed. Wiener JM, ed. Washington, DC: American Psychiatric Press, 1991; 121-127.
-
(1991)
Textbook of Child and Adolescent Psychiatry. 1st Ed.
, pp. 121-127
-
-
Zametkin, A.J.1
Andreason, P.2
Krusei, M.J.P.3
-
55
-
-
0022863056
-
Autism, mental retardation, and chromosomal abnormalities
-
Mariner R, Jackson III AW, Levitas A, Hagerman RJ, Braden M, McBogg PM, Smith ACM, Berry R. Autism, mental retardation, and chromosomal abnormalities. J Autism Dev Disord 1986; 16: 425-40.
-
(1986)
J Autism Dev Disord
, vol.16
, pp. 425-440
-
-
Mariner, R.1
Jackson III, A.W.2
Levitas, A.3
Hagerman, R.J.4
Braden, M.5
McBogg, P.M.6
Smith, A.C.M.7
Berry, R.8
-
56
-
-
0023146037
-
Chromosomal aberrations in 85 mentally retarded patients examined by high resolution banding
-
Tengström C, Autio S. Chromosomal aberrations in 85 mentally retarded patients examined by high resolution banding. Clin Genet 1987; 31: 53-60.
-
(1987)
Clin Genet
, vol.31
, pp. 53-60
-
-
Tengström, C.1
Autio, S.2
|