47,XXX/45,X/46,XX mosaicism in a patient with Turner phenotype and spontaneous puberal development

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Comprar ISCN 2009 - An International System for Human Cytogenetic Nomenclature \| Marilyn L. Slovak \| 9783805589857 \| Karger AG Marilyn L. Slovak, Lisa G. Shaffer BiologyGenetic AnalysisGenetic TestingCytogeneticsMedicine	2009	208
International system for human cytogenetic nomenclature (ISCN) Cancer Genetics and Cytogenetics CytogeneticsGeneticsPathologyInternational SystemMolecular Genetics	1994	142
Gonadal dysgenesis and the Mayer-Rokitansky-Kuster-Hauser syndrome in a girl with 46,X,del(X)(pter→q22:) Sena Aydos, Ajlan Tükün, Işık Bökesoy Archives of Gynecology and Obstetrics Mayer-rokitansky-kuster-hauser SyndromeDevelopmental BiologyGenetic DisorderGeneticsGonadal Dysgenesis	2003	37
X chromosome mosaicism in patients with recurrent abortion or premature ovarian failure. R. C. Wu, Pao‐Lin Kuo, Shujie Lin, PubMed	1993	32
The Mayer–Rokitansky–Kuster–Hauser and gonadal dysgenesis anomaly in a girl with 45,X/46,X,del(X)(p11.21) Ayla Güven, Nurten Kara, Yaman Sağlam, American Journal of Medical Genetics Part A SpermatogenesisDevelopmental AnomalyDevelopmental BiologyGenetic DisorderGenetics	2007	13
Bilateral renal agenesis and Mullerian anomalies in a 47,XXX fetus W. Allen Hogge, Dan J. Vick, P Schnatterly, American Journal of Medical Genetics	1989	13

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