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Items: 17

1.
Klinefelter's syndrome in adolescence.
S. G. Ratcliffe, J. Bancroft, D. Axworthy, W. McLaren
Arch Dis Child. 1982 Jan; 57(1): 6–12.
PMCID:
PMC2863282
SummaryPage BrowsePDF–1.0M
2.
Racial differentials in the prevalence rates of males with sex chromosome abnormalities (XXY, XYY) in security settings in the United States.
E B Hook
Am J Hum Genet. 1974 Jul; 26(4): 504–511.
PMCID:
PMC1762595
SummaryPage BrowsePDF–772K
3.
Klinefelter's syndrome with hypogonadotrophic hypogonadism.
J N Carter, D G Wiseman, H B Lee
Br Med J. 1977 Jan 22; 1(6055): 212. doi: 10.1136/bmj.1.6055.212
PMCID:
PMC1604381
SummaryPage BrowsePDF–226K
4.
Rett syndrome in a boy with a 47,XXY karyotype.
J Salomão Schwartzman, M Zatz, L dos Reis Vasquez, R Ribeiro Gomes, C P Koiffmann, C Fridman, P Guimarães Otto
Am J Hum Genet. 1999 Jun; 64(6): 1781–1785. doi: 10.1086/302424
PMCID:
PMC1377923
SummaryPDF–285K
5.
Klinefelter's syndrome associated with autoimmune disease.
A Schattner, A Berrebi
J R Soc Med. 1989 Sep; 82(9): 560. doi: 10.1177/014107688908200921
PMCID:
PMC1292309
SummaryPage BrowsePDF–226K
6.
Frequency of XY Sperm Increases with Age in Fathers of Boys with Klinefelter Syndrome
Xiu Lowe, Brenda Eskenazi, David O. Nelson, Sharon Kidd, Angela Alme, Andrew J. Wyrobek
Am J Hum Genet. 2001 Nov; 69(5): 1046–1054. Published online 2001 Oct 1. doi: 10.1086/323763
PMCID:
PMC1274351
AbstractArticlePDF–113K
7.
A study of brothers with Klinefelter syndrome.
C G Woods, J Noble, A R Falconer
J Med Genet. 1997 Aug; 34(8): 702. doi: 10.1136/jmg.34.8.702
PMCID:
PMC1051044
SummaryPage BrowsePDF–279K
8.
Incontinentia pigmenti in a boy with Klinefelter's syndrome.
A D Ormerod, M I White, E McKay, A W Johnston
J Med Genet. 1987 Jul; 24(7): 439–441. doi: 10.1136/jmg.24.7.439
PMCID:
PMC1050156
SummaryPage BrowsePDF–359K
9.
Presumptive mosaic origin of an XX/XY female with ambiguous genitalia.
O Zuffardi, L Gargantini, S Lambiase, F Lo Curto, P Maraschio, C E Ford
J Med Genet. 1987 Mar; 24(3): 177–180. doi: 10.1136/jmg.24.3.177
PMCID:
PMC1049955
SummaryPage BrowsePDF–569K
10.
Primary myelodysplastic syndrome with complex chromosomal rearrangements in a patient with Klinefelter's syndrome.
S M Abidi, M Griffiths, D G Oscier, G J Mufti, T J Hamblin
J Med Genet. 1986 Apr; 23(2): 183–185. doi: 10.1136/jmg.23.2.183
PMCID:
PMC1049580
SummaryPage BrowsePDF–582K
11.
Chromosome distribution studies in XXY karyotypes.
M Kirsch-Volders, L Hens, H van den Berghe, B Scholberg, C Susanne
J Med Genet. 1982 Feb; 19(1): 57–62. doi: 10.1136/jmg.19.1.57
PMCID:
PMC1048820
SummaryPage BrowsePDF–865K
12.
Occurrence of Duchenne dystrophy in Klinefelter's syndrome.
V Ramesh, R Mountford, H M Kingston, A Kelsey, M J Noronha, M A Clarke
Arch Dis Child. 1993 Oct; 69(4): 453–454. doi: 10.1136/adc.69.4.453
PMCID:
PMC1029558
SummaryPage BrowsePDF–457K
13.
Becker muscular dystrophy (BMD) and Klinefelter's syndrome: a possible cause of variable expression of BMD within a pedigree.
G K Suthers, J I Manson, L M Stern, E A Haan, J C Mulley
J Med Genet. 1989 Apr; 26(4): 251–254. doi: 10.1136/jmg.26.4.251
PMCID:
PMC1017298
SummaryPage BrowsePDF–701K
14.
Triphalangeal thumb with delta phalanx in a case of Klinefelter's syndrome.
M M Lai, J D Spencer, J A Montandon, A C Berry
J Med Genet. 1991 Jul; 28(7): 497–498. doi: 10.1136/jmg.28.7.497
PMCID:
PMC1016966
SummaryPage BrowsePDF–365K
15.
Probable de novo 17q duplication (q11.2-->q21.1): a newly recognised chromosomal syndrome in a child with Klinefelter's syndrome.
A M Butt, D Mehta, J A Goodeve, F A Flinter
J Med Genet. 1993 May; 30(5): 436–437. doi: 10.1136/jmg.30.5.436
PMCID:
PMC1016388
SummaryPage BrowsePDF–508K
16.
Presence of Brightly Fluorescent Material in Testes of XX Males
Waldemar A. Palutke, Yingsan Chen, Harold Chen
J Med Genet. 1973 Jun; 10(2): 170–174. doi: 10.1136/jmg.10.2.170
PMCID:
PMC1013010
SummaryPage BrowsePDF–1.0M
17.
A case of complete testicular feminisation and 47,XXY karyotype.
M Gerli, G Migliorini, V Bocchini, G Venti, R Ferrarese, E Donti, G Rosi
J Med Genet. 1979 Dec; 16(6): 480–483. doi: 10.1136/jmg.16.6.480
PMCID:
PMC1012597
SummaryPage BrowsePDF–763K

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