-
1
-
-
4344685681
-
Sex chromosomes and brain gender
-
Arnold AP. 2004. Sex chromosomes and brain gender. Nature Rev Neurosci 5: 701-708.
-
(2004)
Nature Rev Neurosci
, vol.5
, pp. 701-708
-
-
Arnold, A.P.1
-
2
-
-
66049159361
-
Psychiatric characteristics in a self-selected sample of boys with Klinefelter syndrome
-
Bruining H, Swaab H, Kas M, van Engeland H. 2009. Psychiatric characteristics in a self-selected sample of boys with Klinefelter syndrome. Pediatrics 123: e865-e870.
-
(2009)
Pediatrics
, vol.123
-
-
Bruining, H.1
Swaab, H.2
Kas, M.3
van Engeland, H.4
-
3
-
-
71849120164
-
Organizational effects of fetal testosterone on human corpus callosum size and asymmetry
-
Chura LR, Lombardo MV, Ashwin E, Auyeung B, Chakrabarti B, Bullmore ET, Baron-Cohen S. 2010. Organizational effects of fetal testosterone on human corpus callosum size and asymmetry. Psychoneuroendocrinology 35: 122-132.
-
(2010)
Psychoneuroendocrinology
, vol.35
, pp. 122-132
-
-
Chura, L.R.1
Lombardo, M.V.2
Ashwin, E.3
Auyeung, B.4
Chakrabarti, B.5
Bullmore, E.T.6
Baron-Cohen, S.7
-
4
-
-
70350519151
-
Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA
-
Coffee B, Keith K, Albizua I, Malone T, Mowrey J, Sherman SL, Warren ST. 2009. Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA. Am J Hum Genet 85: 503-514.
-
(2009)
Am J Hum Genet
, vol.85
, pp. 503-514
-
-
Coffee, B.1
Keith, K.2
Albizua, I.3
Malone, T.4
Mowrey, J.5
Sherman, S.L.6
Warren, S.T.7
-
5
-
-
0022036826
-
Sex chromosome variations in school-age children
-
Cohen FL, Durham JD. 1985. Sex chromosome variations in school-age children. J Sch Health 55: 99-102.
-
(1985)
J Sch Health
, vol.55
, pp. 99-102
-
-
Cohen, F.L.1
Durham, J.D.2
-
6
-
-
0025201716
-
Brief report: A 48XXXY/49XXXXY male with expressive speech defect
-
Collacott RA, Mitchell C, Dawes-Gamble L, Young ID, Duckett D. 1990. Brief report: A 48XXXY/49XXXXY male with expressive speech defect. J Autism Dev Disord 20: 577-580.
-
(1990)
J Autism Dev Disord
, vol.20
, pp. 577-580
-
-
Collacott, R.A.1
Mitchell, C.2
Dawes-Gamble, L.3
Young, I.D.4
Duckett, D.5
-
7
-
-
0041821565
-
Clinical findings and phenotype in a toddler with 48, XXYY syndrome
-
Demirhan O. 2003. Clinical findings and phenotype in a toddler with 48, XXYY syndrome. Am J Med Genet Part A. 119A: 393-394.
-
(2003)
Am J Med Genet Part A.
, vol.119 A
, pp. 393-394
-
-
Demirhan, O.1
-
8
-
-
17744392634
-
Klinefelter's syndrome (XXY) as a genetic model for psychotic disorders
-
DeLisi LE, Maurizio AM, Svetina C, Ardekani B, Szulc K, Nierenberg J, Leonard J, Harvey PD. 2005. Klinefelter's syndrome (XXY) as a genetic model for psychotic disorders. Am J Med Genet Part B 135B: 15-23.
-
(2005)
Am J Med Genet Part B
, vol.135 B
, pp. 15-23
-
-
DeLisi, L.E.1
Maurizio, A.M.2
Svetina, C.3
Ardekani, B.4
Szulc, K.5
Nierenberg, J.6
Leonard, J.7
Harvey, P.D.8
-
9
-
-
0026546540
-
48,XXYY syndrome in a boy with essential tremor. Comparison with 120 cases from the literature
-
Donati F, Gasser S, Mullis P, Braga S, Vassella F. 1992. 48, XXYY syndrome in a boy with essential tremor. Comparison with 120 cases from the literature. Monatsschr Kinderheilkd 140: 216-219.
-
(1992)
Monatsschr Kinderheilkd
, vol.140
, pp. 216-219
-
-
Donati, F.1
Gasser, S.2
Mullis, P.3
Braga, S.4
Vassella, F.5
-
10
-
-
0020372049
-
A cytogenetic survey of 14,069 newborn infants. IV. Further follow-up on the children with sex chromosome anomalies
-
Evans JA, de von Flindt R, Greenberg C, Ramsay S, Hamerton JL. 1982. A cytogenetic survey of 14, 069 newborn infants. IV. Further follow-up on the children with sex chromosome anomalies. Birth Defects Orig Artic Ser 18: 169-184.
-
(1982)
Birth Defects Orig Artic Ser
, vol.18
, pp. 169-184
-
-
Evans, J.A.1
de von Flindt, R.2
Greenberg, C.3
Ramsay, S.4
Hamerton, J.L.5
-
11
-
-
0029056142
-
XYY syndrome and other Y chromosome polysomies. Mental status and psychosocial functioning
-
Fryns JP, Kleczkowska A, Kubień E, Van den Berghe H. 1995. XYY syndrome and other Y chromosome polysomies. Mental status and psychosocial functioning. Genet Couns 6: 197-206.
-
(1995)
Genet Couns
, vol.6
, pp. 197-206
-
-
Fryns, J.P.1
Kleczkowska, A.2
Kubień, E.3
Van den Berghe, H.4
-
12
-
-
0016806814
-
Case studies of three "XXYY" children
-
Garvey M, Kellett B. 1975. Case studies of three "XXYY" children. Br J Disord Commun 10: 17-30.
-
(1975)
Br J Disord Commun
, vol.10
, pp. 17-30
-
-
Garvey, M.1
Kellett, B.2
-
13
-
-
34247096894
-
Androgens and the brain
-
Genazzani AR, Pluchino N, Freschi L, Ninni F, Luisi M. 2007. Androgens and the brain. Maturitas 57: 27-30.
-
(2007)
Maturitas
, vol.57
, pp. 27-30
-
-
Genazzani, A.R.1
Pluchino, N.2
Freschi, L.3
Ninni, F.4
Luisi, M.5
-
14
-
-
0031454574
-
Sexual dimorphism of the developing human brain
-
Giedd JN, Castellanos FX, Rajapakse JC, Vaituzis AC, Rapoport JL. 1997. Sexual dimorphism of the developing human brain. Prog Neuropsychopharmacol Biol Psychiatry 21: 1185-1201.
-
(1997)
Prog Neuropsychopharmacol Biol Psychiatry
, vol.21
, pp. 1185-1201
-
-
Giedd, J.N.1
Castellanos, F.X.2
Rajapakse, J.C.3
Vaituzis, A.C.4
Rapoport, J.L.5
-
15
-
-
33846914971
-
XXY (Klinefelter syndrome): A pediatric quantitative brain magnetic resonance imaging case-control study
-
Giedd JN, Clasen L, Wallace G, Lenroot RK, Lerch JP, Wells EM, Blumenthal JD, Nelson JE, Tossell JW, Stayer C, Evans AC, Samango-Sprouse CA. 2007. XXY (Klinefelter syndrome): A pediatric quantitative brain magnetic resonance imaging case-control study. Pediatrics 119: e232-e240.
-
(2007)
Pediatrics
, vol.119
-
-
Giedd, J.N.1
Clasen, L.2
Wallace, G.3
Lenroot, R.K.4
Lerch, J.P.5
Wells, E.M.6
Blumenthal, J.D.7
Nelson, J.E.8
Tossell, J.W.9
Stayer, C.10
Evans, A.C.11
Samango-Sprouse, C.A.12
-
16
-
-
69249219068
-
Molecular studies of a patient with complete androgen insensitivity and a 47, XXY karyotype
-
Girardin CM, Deal C, Lemyre E, Paquette J, Lumbroso R, Beitel LK, Trifiro MA, Van Vliet G. 2009. Molecular studies of a patient with complete androgen insensitivity and a 47, XXY karyotype. J Pediatr 155: 439-443.
-
(2009)
J Pediatr
, vol.155
, pp. 439-443
-
-
Girardin, C.M.1
Deal, C.2
Lemyre, E.3
Paquette, J.4
Lumbroso, R.5
Beitel, L.K.6
Trifiro, M.A.7
Van Vliet, G.8
-
17
-
-
77952769435
-
Clinical variability and novel neurodevelopmental findings in 49, XXXXY syndrome
-
Gropman AL, Rogol A, Fennoy I, Sadeghin T, Sinn S, Jameson R, Mitchell F, Clabaugh J, Lutz-Armstrong M, Samango-Sprouse CA. 2010. Clinical variability and novel neurodevelopmental findings in 49, XXXXY syndrome. Am J Med Genet Part A 152A: 1523-1530.
-
(2010)
Am J Med Genet Part A
, vol.152 A
, pp. 1523-1530
-
-
Gropman, A.L.1
Rogol, A.2
Fennoy, I.3
Sadeghin, T.4
Sinn, S.5
Jameson, R.6
Mitchell, F.7
Clabaugh, J.8
Lutz-Armstrong, M.9
Samango-Sprouse, C.A.10
-
18
-
-
38449087657
-
The origin of human aneuploidy: Where we have been, where we are going
-
Hassold TJ, Hall H, Hunt P. 2007. The origin of human aneuploidy: Where we have been, where we are going. Hum Mol Genet 16: R203-R208.
-
(2007)
Hum Mol Genet
, vol.16
-
-
Hassold, T.J.1
Hall, H.2
Hunt, P.3
-
19
-
-
0015079966
-
49, XXXXY chromosomal anomaly in a neonate
-
Hayek A, Riccardi V, Atkins L, Hendren H. 1971. 49, XXXXY chromosomal anomaly in a neonate. J Med Genet 8: 220-221.
-
(1971)
J Med Genet
, vol.8
, pp. 220-221
-
-
Hayek, A.1
Riccardi, V.2
Atkins, L.3
Hendren, H.4
-
20
-
-
33845434242
-
Prenatal testosterone and gender-related behaviour
-
Hines M. 2006. Prenatal testosterone and gender-related behaviour Eur J Endocrinol 155: S115-S121.
-
(2006)
Eur J Endocrinol
, vol.155
-
-
Hines, M.1
-
21
-
-
43449114177
-
Brain magnetic resonance imaging findings in 49, XXXXY syndrome
-
Hoffman TL, Vossough A, Ficicioglu C, Visootsak J. 2008. Brain magnetic resonance imaging findings in 49, XXXXY syndrome. Pediatr Neurol 38: 450-453.
-
(2008)
Pediatr Neurol
, vol.38
, pp. 450-453
-
-
Hoffman, T.L.1
Vossough, A.2
Ficicioglu, C.3
Visootsak, J.4
-
22
-
-
33646027042
-
The structural brain correlates of cognitive deficits in adults with Klinefelter's syndrome
-
Itti E. 2006. The structural brain correlates of cognitive deficits in adults with Klinefelter's syndrome. J Clin Endocrinol Metab 91: 1423-1427.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, pp. 1423-1427
-
-
Itti, E.1
-
23
-
-
0242353068
-
Functional neuroimaging provides evidence of anomalous cerebral laterality in adults with Klinefelter's syndrome
-
Itti E, Gaw Gonzalo IT, Boone KB, Geschwind DH, Berman N, Pawlikowska-Haddal A, Itti L, Mishkin FS, Swerdloff RS. 2003. Functional neuroimaging provides evidence of anomalous cerebral laterality in adults with Klinefelter's syndrome. Ann Neurol 54: 669-673.
-
(2003)
Ann Neurol
, vol.54
, pp. 669-673
-
-
Itti, E.1
Gaw Gonzalo, I.T.2
Boone, K.B.3
Geschwind, D.H.4
Berman, N.5
Pawlikowska-Haddal, A.6
Itti, L.7
Mishkin, F.S.8
Swerdloff, R.S.9
-
24
-
-
0034198366
-
Improvement of peripheral neuropathy by testosterone in a patient with 48, XXYY syndrome
-
Izumi S, Tsubahara A. 2000. Improvement of peripheral neuropathy by testosterone in a patient with 48, XXYY syndrome. Tokai J Exp Clin Med 25: 39-44.
-
(2000)
Tokai J Exp Clin Med
, vol.25
, pp. 39-44
-
-
Izumi, S.1
Tsubahara, A.2
-
25
-
-
0023746674
-
X-chromosome polysomy in the male. The Leuven experience 1966-1987
-
Kleczkowska A, Fryns JP, Van den Berghe H. 1988. X-chromosome polysomy in the male. The Leuven experience 1966-1987. Hum Genet 80: 16-22.
-
(1988)
Hum Genet
, vol.80
, pp. 16-22
-
-
Kleczkowska, A.1
Fryns, J.P.2
Van den Berghe, H.3
-
26
-
-
33750627525
-
Fetal testosterone and sex differences in typical social development and in autism
-
Knickmeyer RC, Baron-Cohen S. 2006. Fetal testosterone and sex differences in typical social development and in autism. J Child Neurol 21: 825-845.
-
(2006)
J Child Neurol
, vol.21
, pp. 825-845
-
-
Knickmeyer, R.C.1
Baron-Cohen, S.2
-
28
-
-
0027994243
-
Parental origin of the extra chromosomes in polysomy X
-
Leal CA, Belmont JW, Nachtman R, Cantu JM, Medina C. 1994. Parental origin of the extra chromosomes in polysomy X. Hum Genet 94: 423-426.
-
(1994)
Hum Genet
, vol.94
, pp. 423-426
-
-
Leal, C.A.1
Belmont, J.W.2
Nachtman, R.3
Cantu, J.M.4
Medina, C.5
-
29
-
-
75349108961
-
Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: A systematic review
-
Leggett V, Jacobs P, Nation K, Scerif G, Bishop DV. 2010. Neurocognitive outcomes of individuals with a sex chromosome trisomy: XXX, XYY, or XXY: A systematic review. Dev Med Child Neurol 52: 119-129.
-
(2010)
Dev Med Child Neurol
, vol.52
, pp. 119-129
-
-
Leggett, V.1
Jacobs, P.2
Nation, K.3
Scerif, G.4
Bishop, D.V.5
-
30
-
-
73849105651
-
Effects of sex chromosome aneuploidies on brain development: Evidence from neuroimaging studies
-
Lenroot RK, Lee NR, Giedd JN. 2009. Effects of sex chromosome aneuploidies on brain development: Evidence from neuroimaging studies. Dev Disabil Res Rev 15: 318-327.
-
(2009)
Dev Disabil Res Rev
, vol.15
, pp. 318-327
-
-
Lenroot, R.K.1
Lee, N.R.2
Giedd, J.N.3
-
32
-
-
0001611628
-
Abnormalities of sex chromosome constitution in newborn babies
-
MacLean N, Harnden DG, Court Brown WM. 1961. Abnormalities of sex chromosome constitution in newborn babies. Lancet 2: 406-408.
-
(1961)
Lancet
, vol.2
, pp. 406-408
-
-
MacLean, N.1
Harnden, D.G.2
Court Brown, W.M.3
-
33
-
-
33744949778
-
Adaptive and maladaptive behavior in children with Smith-Magenis syndrome
-
Martin SC, Wolters PL, Smith AC. 2006. Adaptive and maladaptive behavior in children with Smith-Magenis syndrome. J Autism Dev Disord 36: 541-552.
-
(2006)
J Autism Dev Disord
, vol.36
, pp. 541-552
-
-
Martin, S.C.1
Wolters, P.L.2
Smith, A.C.3
-
34
-
-
0015863286
-
49, XXXXY karyotype in mentally retarded boy
-
Morić-Petrović S, Laca Z, Marković S, Marković V. 1973. 49, XXXXY karyotype in mentally retarded boy. J Ment Defic Res 17: 73-80.
-
(1973)
J Ment Defic Res
, vol.17
, pp. 73-80
-
-
Morić-Petrović, S.1
Laca, Z.2
Marković, S.3
Marković, V.4
-
35
-
-
0022843186
-
Summary overview of behavioural development in individuals with neonatally identified X and Y aneuploidy
-
Netley CT. 1986. Summary overview of behavioural development in individuals with neonatally identified X and Y aneuploidy. Birth Defects Orig Artic Ser 22: 293-306.
-
(1986)
Birth Defects Orig Artic Ser
, vol.22
, pp. 293-306
-
-
Netley, C.T.1
-
36
-
-
0025542292
-
Sex chromosome abnormalities found among 34,910 newborn children: Results from a 13-year incidence study in Arhus, Denmark
-
Nielsen J, Wohlert M. 1990. Sex chromosome abnormalities found among 34, 910 newborn children: Results from a 13-year incidence study in Arhus, Denmark. Birth Defects Orig Artic Ser 26: 209-223.
-
(1990)
Birth Defects Orig Artic Ser
, vol.26
, pp. 209-223
-
-
Nielsen, J.1
Wohlert, M.2
-
37
-
-
0023261248
-
Follow-up 20 years later of 34 Klinefelter males with karyotype 47, XXY and 16 hypogonadal males with karyotype 46,XY
-
Nielsen J, Pelsen B. 1987. Follow-up 20 years later of 34 Klinefelter males with karyotype 47, XXY and 16 hypogonadal males with karyotype 46, XY Hum Genet 77: 188-192.
-
(1987)
Hum Genet
, vol.77
, pp. 188-192
-
-
Nielsen, J.1
Pelsen, B.2
-
38
-
-
0028145087
-
The 48, XXYY syndrome: A case detected by maternal serum alpha-fetoprotein screening
-
Nyberg RH, Karhu R, Karikoski R, Simola KO. 1994. The 48, XXYY syndrome: A case detected by maternal serum alpha-fetoprotein screening. Prenat Diagn 14: 644-645.
-
(1994)
Prenat Diagn
, vol.14
, pp. 644-645
-
-
Nyberg, R.H.1
Karhu, R.2
Karikoski, R.3
Simola, K.O.4
-
39
-
-
0020214534
-
49, XXXXY syndrome
-
Pallister PD. 1982. 49, XXXXY syndrome. Am J Med Genet 13: 337-339.
-
(1982)
Am J Med Genet
, vol.13
, pp. 337-339
-
-
Pallister, P.D.1
-
40
-
-
0034720808
-
Brain morphology in Klinefelter syndrome: Extra X chromosome and testosterone supplementation
-
Patwardhan AJ, Eliez S, Bender B, Linden MG, Reiss AL. 2000. Brain morphology in Klinefelter syndrome: Extra X chromosome and testosterone supplementation. Neurology 54: 2218-2223.
-
(2000)
Neurology
, vol.54
, pp. 2218-2223
-
-
Patwardhan, A.J.1
Eliez, S.2
Bender, B.3
Linden, M.G.4
Reiss, A.L.5
-
41
-
-
48049118700
-
Reduced size of the amygdala in individuals with 47,XXY and 47, XXX karyotypes
-
Patwardhan A, Brown W, Bender B, Linden MG, Eliez S, Reiss AL. 2002. Reduced size of the amygdala in individuals with 47, XXY and 47, XXX karyotypes. Am J Med Genet 114: 93-98.
-
(2002)
Am J Med Genet
, vol.114
, pp. 93-98
-
-
Patwardhan, A.1
Brown, W.2
Bender, B.3
Linden, M.G.4
Eliez, S.5
Reiss, A.L.6
-
42
-
-
0031899204
-
49, XXXXY: A distinct phenotype. Three new cases and review
-
Peet J, Weaver D, Vance G. 1998. 49, XXXXY: A distinct phenotype. Three new cases and review. J Med Genet 35: 420-424.
-
(1998)
J Med Genet
, vol.35
, pp. 420-424
-
-
Peet, J.1
Weaver, D.2
Vance, G.3
-
43
-
-
0020040614
-
Speech and learning disorders in children with sex chromosome abnormalities
-
Ratcliffe SG. 1982. Speech and learning disorders in children with sex chromosome abnormalities. Dev Med Child Neurol 24: 80-84.
-
(1982)
Dev Med Child Neurol
, vol.24
, pp. 80-84
-
-
Ratcliffe, S.G.1
-
44
-
-
0018415758
-
Additional pedigree supporting the frequent origin of XXYY from consecutive meiotic non-disjunction in paternal gametogenesis
-
Rinaldi A, Archidiacono N, Rocchi M, Filippi G. 1979. Additional pedigree supporting the frequent origin of XXYY from consecutive meiotic non-disjunction in paternal gametogenesis. J Med Genet 16: 225-226.
-
(1979)
J Med Genet
, vol.16
, pp. 225-226
-
-
Rinaldi, A.1
Archidiacono, N.2
Rocchi, M.3
Filippi, G.4
-
46
-
-
40449140662
-
Cognitive and motor development during childhood in boys with Klinefelter syndrome
-
Ross JL, Roeltgen DP, Stefanatos G, Benecke R, Zeger MP, Kushner H, Ramos P, Elder FF, Zinn AR. 2008. Cognitive and motor development during childhood in boys with Klinefelter syndrome. Am J Med Genet Part A 146A: 708-719.
-
(2008)
Am J Med Genet Part A
, vol.146 A
, pp. 708-719
-
-
Ross, J.L.1
Roeltgen, D.P.2
Stefanatos, G.3
Benecke, R.4
Zeger, M.P.5
Kushner, H.6
Ramos, P.7
Elder, F.F.8
Zinn, A.R.9
-
47
-
-
0028843850
-
Intelligence and achievement in children with extra X aneuploidy: A longitudinal perspective
-
Rovet J, Netley C, Bailey J, Keenan M, Stewart D. 1995. Intelligence and achievement in children with extra X aneuploidy: A longitudinal perspective. Am J Med Genet 60: 356-363.
-
(1995)
Am J Med Genet
, vol.60
, pp. 356-363
-
-
Rovet, J.1
Netley, C.2
Bailey, J.3
Keenan, M.4
Stewart, D.5
-
48
-
-
0030093046
-
The psychoeducational profile of boys with Klinefelter syndrome
-
Rovet J, Netley C, Keenan M, Bailey J, Stewart D. 1996. The psychoeducational profile of boys with Klinefelter syndrome. J Learn Disabil 29: 180-196.
-
(1996)
J Learn Disabil
, vol.29
, pp. 180-196
-
-
Rovet, J.1
Netley, C.2
Keenan, M.3
Bailey, J.4
Stewart, D.5
-
49
-
-
0034843903
-
Mental development in polysomy X Klinefelter syndrome (47, XXY; 48, XXXY): Effects of incomplete X inactivation
-
Samango-Sprouse C. 2001. Mental development in polysomy X Klinefelter syndrome (47, XXY; 48, XXXY): Effects of incomplete X inactivation. Semin Reprod Med 19: 193-202.
-
(2001)
Semin Reprod Med
, vol.19
, pp. 193-202
-
-
Samango-Sprouse, C.1
-
50
-
-
0036057356
-
XXY the hidden disability and a prototype for an infantile presentation of developmental dyspraxia (IDD)
-
Samango-Sprouse C, Rogol A. 2002. XXY the hidden disability and a prototype for an infantile presentation of developmental dyspraxia (IDD) Infants Young Child 15: 11-18.
-
(2002)
Infants Young Child
, vol.15
, pp. 11-18
-
-
Samango-Sprouse, C.1
Rogol, A.2
-
51
-
-
79955521590
-
Effects of short-course androgen therapy on the neurodevelopmental profile of infants and children with 49, XXXXY syndrome
-
Samango-Sprouse CA, Gropman AL, Sadeghin T, Kingery M, Lutz-Armstrong M, Rogol AD. 2011. Effects of short-course androgen therapy on the neurodevelopmental profile of infants and children with 49, XXXXY syndrome. Acta Paediat 100: 861-865.
-
(2011)
Acta Paediat
, vol.100
, pp. 861-865
-
-
Samango-Sprouse, C.A.1
Gropman, A.L.2
Sadeghin, T.3
Kingery, M.4
Lutz-Armstrong, M.5
Rogol, A.D.6
-
52
-
-
84873076662
-
Positive effects of short course androgen therapy on the neurodevelopmental outcome in boys with 47, XXY syndrome at 36 and 72 months of age
-
in press).
-
Samango-Sprouse CA, Sadeghin T, Mitchell FL, Dixon T, Stapleton E, Kingery M, Gropman AL. Positive effects of short course androgen therapy on the neurodevelopmental outcome in boys with 47, XXY syndrome at 36 and 72 months of age. Am J Med Gen (in press).
-
Am J Med Gen
-
-
Samango-Sprouse, C.A.1
Sadeghin, T.2
Mitchell, F.L.3
Dixon, T.4
Stapleton, E.5
Kingery, M.6
Gropman, A.L.7
-
55
-
-
10744225919
-
Klinefelter syndrome: Expanding the phenotype and identifying new research directions
-
Simpson JL, de la Cruz F, Swerdloff RS, Samango-Sprouse C, Skakkebaek NE, Graham JM Jr, Hassold T, Aylstock M, Meyer-Bahlburg HF, Willard HF, Hall JG, Salameh W, Boone K, Staessen C, Geschwind D, Giedd J, Dobs AS, Rogol A, Brinton B, Paulsen CA. 2003. Klinefelter syndrome: Expanding the phenotype and identifying new research directions. Genet Med 5: 460-468.
-
(2003)
Genet Med
, vol.5
, pp. 460-468
-
-
Simpson, J.L.1
de la Cruz, F.2
Swerdloff, R.S.3
Samango-Sprouse, C.4
Skakkebaek, N.E.5
Graham Jr., J.M.6
Hassold, T.7
Aylstock, M.8
Meyer-Bahlburg, H.F.9
Willard, H.F.10
Hall, J.G.11
Salameh, W.12
Boone, K.13
Staessen, C.14
Geschwind, D.15
Giedd, J.16
Dobs, A.S.17
Rogol, A.18
Brinton, B.19
Paulsen, C.A.20
more..
-
56
-
-
17444421587
-
X-linked genes and mental functioning
-
Skuse DH. 2005. X-linked genes and mental functioning. Hum Mol Genet 14: R27-R32.
-
(2005)
Hum Mol Genet
, vol.14
-
-
Skuse, D.H.1
-
57
-
-
0026656886
-
Physical and mental development of adolescent males with Klinefelter syndrome
-
Sørensen K. 1992. Physical and mental development of adolescent males with Klinefelter syndrome. Horm Res 37: 55-61.
-
(1992)
Horm Res
, vol.37
, pp. 55-61
-
-
Sørensen, K.1
-
58
-
-
0018010481
-
The 48, XXYY syndrome
-
Sørensen K, Nielsen J, Jacobsen P, Rolle T. 1978. The 48, XXYY syndrome. J Ment Defic Res 22: 197-205.
-
(1978)
J Ment Defic Res
, vol.22
, pp. 197-205
-
-
Sørensen, K.1
Nielsen, J.2
Jacobsen, P.3
Rolle, T.4
-
59
-
-
73849125375
-
Structural and functional neuroimaging in Klinefelter (47, XXY) syndrome: A review of the literature and preliminary results from a functional magnetic resonance imaging study of language
-
Steinman K, Ross J, Lai S, Reiss A, Hoeft F. 2009. Structural and functional neuroimaging in Klinefelter (47, XXY) syndrome: A review of the literature and preliminary results from a functional magnetic resonance imaging study of language. Dev Disabil Res Rev 15: 295-308.
-
(2009)
Dev Disabil Res Rev
, vol.15
, pp. 295-308
-
-
Steinman, K.1
Ross, J.2
Lai, S.3
Reiss, A.4
Hoeft, F.5
-
60
-
-
44849133641
-
A new look at XXYY syndrome: Medical and psychological features
-
Tartaglia N, Davis S, Hench A, Nimishakavi S, Beauregard R, Reynolds A, Fenton L, Albrecht L, Ross J, Visootsak J, Hansen R, Hagerman R. 2008. A new look at XXYY syndrome: Medical and psychological features. Am J Med Genet Part A 146A: 1509-1522.
-
(2008)
Am J Med Genet Part A
, vol.146 A
, pp. 1509-1522
-
-
Tartaglia, N.1
Davis, S.2
Hench, A.3
Nimishakavi, S.4
Beauregard, R.5
Reynolds, A.6
Fenton, L.7
Albrecht, L.8
Ross, J.9
Visootsak, J.10
Hansen, R.11
Hagerman, R.12
-
61
-
-
79955524495
-
48, XXYY, 48, XXXY and 49, XXXXY syndromes: Not just variants of Klinefelter syndrome
-
Tartaglia N, Ayari N, Howell S, D'Epagnier C, Zeitler P. 2011. 48, XXYY, 48, XXXY and 49, XXXXY syndromes: Not just variants of Klinefelter syndrome. Acta Paediatr 100: 851-860.
-
(2011)
Acta Paediatr
, vol.100
, pp. 851-860
-
-
Tartaglia, N.1
Ayari, N.2
Howell, S.3
D'Epagnier, C.4
Zeitler, P.5
-
62
-
-
84865144084
-
The construct of adaptive behavior: Its conceptualization, measurement, and use in the field of intellectual disability
-
Tassé MJ, Schalock RL, Balboni G, Bersani H Jr, Borthwick-Duffy SA, Spreat S, Thissen D, Widaman KF, Zhang D. 2012. The construct of adaptive behavior: Its conceptualization, measurement, and use in the field of intellectual disability. Am J Intellect Dev Disabil 117: 291-303.
-
(2012)
Am J Intellect Dev Disabil
, vol.117
, pp. 291-303
-
-
Tassé, M.J.1
Schalock, R.L.2
Balboni, G.3
Bersani Jr., H.4
Borthwick-Duffy, S.A.5
Spreat, S.6
Thissen, D.7
Widaman, K.F.8
Zhang, D.9
-
63
-
-
33750589017
-
Klinefelter's syndrome (karyotype 47, XXY) and schizophrenia-spectrum pathology
-
van Rijn S, Aleman A, Swaab H, Kahn R. 2006. Klinefelter's syndrome (karyotype 47, XXY) and schizophrenia-spectrum pathology. Br J Psychiatry 189: 459-460.
-
(2006)
Br J Psychiatry
, vol.189
, pp. 459-460
-
-
van Rijn, S.1
Aleman, A.2
Swaab, H.3
Kahn, R.4
-
64
-
-
43049146124
-
Effects of an extra X chromosome on language lateralization: An fMRI study with Klinefelter men (47, XXY)
-
van Rijn S, Aleman A, Swaab H, Vink M, Sommer I, Kahn RS. 2008. Effects of an extra X chromosome on language lateralization: An fMRI study with Klinefelter men (47, XXY) Schizophr Res 101: 17-25.
-
(2008)
Schizophr Res
, vol.101
, pp. 17-25
-
-
van Rijn, S.1
Aleman, A.2
Swaab, H.3
Vink, M.4
Sommer, I.5
Kahn, R.S.6
-
65
-
-
0021443805
-
Mental illness, epilepsy and hypothyroidism in XXYY syndrome
-
Vanyan M. 1984. Mental illness, epilepsy and hypothyroidism in XXYY syndrome. Br J Psychiatry 144: 668.
-
(1984)
Br J Psychiatry
, vol.144
, pp. 668
-
-
Vanyan, M.1
-
66
-
-
10744226630
-
Gender-specific gene expression in postmortem human brain: Localization to sex chromosomes
-
Vawter MP, Evans S, Choudary P, Tomita H, Meador-Woodruff J, Molnar M, Li J, Lopez JF, Myers F. 2004. Gender-specific gene expression in postmortem human brain: Localization to sex chromosomes. Neuropsychopharmacology 29: 373-384.
-
(2004)
Neuropsychopharmacology
, vol.29
, pp. 373-384
-
-
Vawter, M.P.1
Evans, S.2
Choudary, P.3
Tomita, H.4
Meador-Woodruff, J.5
Molnar, M.6
Li, J.7
Lopez, J.F.8
Myers, F.9
-
67
-
-
77953928072
-
Klinefelter's syndrome and psychoneurologic function
-
Verri A, Cremante A, Clerici F, Destefani V, Radicioni A. 2010. Klinefelter's syndrome and psychoneurologic function. Mol Hum Reprod 16: 425-433.
-
(2010)
Mol Hum Reprod
, vol.16
, pp. 425-433
-
-
Verri, A.1
Cremante, A.2
Clerici, F.3
Destefani, V.4
Radicioni, A.5
-
68
-
-
34248156426
-
Klinefelter syndrome and other sex chromosomal aneuploidies
-
Visootsak J, Graham JM Jr. 2006. Klinefelter syndrome and other sex chromosomal aneuploidies. Orphanet J Rare Dis 24: 42.
-
(2006)
Orphanet J Rare Dis
, vol.24
, pp. 42
-
-
Visootsak, J.1
Graham Jr., J.M.2
-
69
-
-
34249885593
-
Behavioral phenotype of sex chromosome aneuploidies: 48, XXYY, 48, XXXY, and 49, XXXXY
-
Visootsak J, Rosner B, Dykens E, Tartaglia N, Graham JM Jr. 2007. Behavioral phenotype of sex chromosome aneuploidies: 48, XXYY, 48, XXXY, and 49, XXXXY. Am J Med Genet Part A 143A: 1198-1203.
-
(2007)
Am J Med Genet Part A
, vol.143 A
, pp. 1198-1203
-
-
Visootsak, J.1
Rosner, B.2
Dykens, E.3
Tartaglia, N.4
Graham Jr., J.M.5
-
70
-
-
0032892282
-
Volumetric magnetic resonance imaging study of the brain in subjects with sex chromosome aneuploidies
-
Warwick MM, Doody GA, Lawrie SM, Kestelman JN, Best JJ, Johnstone EC. 1999. Volumetric magnetic resonance imaging study of the brain in subjects with sex chromosome aneuploidies. J Neurol Neurosurg Psychiatry 66: 628-632.
-
(1999)
J Neurol Neurosurg Psychiatry
, vol.66
, pp. 628-632
-
-
Warwick, M.M.1
Doody, G.A.2
Lawrie, S.M.3
Kestelman, J.N.4
Best, J.J.5
Johnstone, E.C.6
-
71
-
-
65649142582
-
Transcriptome analysis of male-female differences in prefrontal cortical development
-
Weickert CS, Elashoff M, Richards AB, Sinclair D, Bahn S, Paabo S, Khaitovich P, Webster MJ. 2009. Transcriptome analysis of male-female differences in prefrontal cortical development. Mol Psychiatry 14: 558-561.
-
(2009)
Mol Psychiatry
, vol.14
, pp. 558-561
-
-
Weickert, C.S.1
Elashoff, M.2
Richards, A.B.3
Sinclair, D.4
Bahn, S.5
Paabo, S.6
Khaitovich, P.7
Webster, M.J.8
-
72
-
-
0019209886
-
XXYY syndrome discovered on routine physical examination
-
Zack BG. 1990. XXYY syndrome discovered on routine physical examination. J Adolesc Health Care 1: 60-62.
-
(1990)
J Adolesc Health Care
, vol.1
, pp. 60-62
-
-
Zack, B.G.1
-
73
-
-
0344823806
-
Two 48, XXYY patients: Clinical, cytogenetic and molecular aspects
-
Zelante L, Piemontese MR, Francioli G, Calvano S. 2003. Two 48, XXYY patients: Clinical, cytogenetic and molecular aspects. Ann Genet 46: 479-481.
-
(2003)
Ann Genet
, vol.46
, pp. 479-481
-
-
Zelante, L.1
Piemontese, M.R.2
Francioli, G.3
Calvano, S.4
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