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Phenotypic effects of mosaicism for a 47,XXX cell line in Turner syndromeSybert, V PJournal of medical genetics, 2002-03, Vol.39 (3), p.217-221 [Periódico revisado por pares]London: BMJ Publishing Group LtdTexto completo disponível |
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Phenotype, ovarian function, and growth in patients with 45,X/47,XXX Turner mosaicism: Implications for prenatal counseling and estrogen therapy at pubertyBlair, Joanne ; Tolmie, John ; Hollman, Anne S. ; Donaldson, Malcolm D.C.The Journal of pediatrics, 2001-11, Vol.139 (5), p.724-728 [Periódico revisado por pares]New York, NY: Mosby, IncTexto completo disponível |
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47,XXX male: A clinical and molecular studyOgata, Tsutomu ; Matsuo, Mari ; Muroya, Koji ; Koyama, Yasuhiro ; Fukutani, KeikoAmerican journal of medical genetics, 2001-02, Vol.98 (4), p.353-356 [Periódico revisado por pares]New York: John Wiley & Sons, IncTexto completo disponível |
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Normal growth and normalization of hypergonadotropic hypogonadism in atypical turner syndrome (45,X/46,XX/47,XXX) : correlation of body height with distribution of cell linesPARTSCH, C.-J ; PANKAU, R ; SIPPELL, W. G ; TOLKSDORF, MEuropean journal of pediatrics, 1994-06, Vol.153 (6), p.451-455 [Periódico revisado por pares]Heidelberg: SpringerTexto completo disponível |
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Psychosocial competence of unselected young adults with sex chromosome abnormalitiesBender, Bruce G. ; Harmon, Robert J. ; Linden, Mary G. ; Bucher-Bartelson, Becki ; Robinson, ArthurAmerican journal of medical genetics, 1999-04, Vol.88 (2), p.200-206 [Periódico revisado por pares]New York: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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Material Type: Artigo
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Analysis of two 47,XXX males reveals X-Y interchange and maternal or paternal nondisjunctionSCHERER, G ; SCHEMPP, W ; FRACCARO, M ; BAUSCH, E ; BIGOZZI, V ; MARASCHIO, P ; MONTALI, E ; SIMONI, G ; WOLF, UHuman genetics, 1989-02, Vol.81 (3), p.247-251 [Periódico revisado por pares]Heidelberg: SpringerTexto completo disponível |
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Genetic counseling for sex chromosome abnormalitiesLinden, Mary G. ; Bender, Bruce G. ; Robinson, ArthurAmerican journal of medical genetics, 2002-06, Vol.110 (1), p.3-10New York: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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Fifty-one prenatally diagnosed children and adolescents with sex chromosome abnormalitiesLinden, Mary G. ; Bender, Bruce G.American journal of medical genetics, 2002-06, Vol.110 (1), p.11-18New York: Wiley Subscription Services, Inc., A Wiley CompanyTexto completo disponível |
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Low rates of pregnancy termination for prenatally diagnosed Klinefelter syndrome and other sex chromosome polysomiesMeschede, Dieter ; Louwen, Frank ; Nippert, Irmgard ; Holzgreve, Wolfgang ; Miny, Peter ; Horst, JürgenAmerican journal of medical genetics, 1998-12, Vol.80 (4), p.330-334New York: John Wiley & Sons, IncTexto completo disponível |
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Material Type: Artigo
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Is the prevalence of Klinefelter syndrome increasing?MORRIS, Joan K ; ALBERMAN, Eva ; SCOTT, Claire ; JACOBS, PatriciaEuropean journal of human genetics : EJHG, 2008-02, Vol.16 (2), p.163-170 [Periódico revisado por pares]Avenel, NJ: Nature PublishingTexto completo disponível |