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Hungarian Medical Journal
Authors: László Ságodi, Enikő Sólyom, András Tóth, Anna Kékesi, Erika P. Tardy, Éva Borbás, Teofil Rétfalvi, Ákos Kiss, and Anikó Korcsmáros

8 Hernando, C., Carrera, M., Ribas, I. et al.: Prenatal and postnatal characterization of Y chromosome structural anomalies by molecular cytogenetic analysis. Prenat. Diagn

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Orvosi Hetilap
Authors: László Ságodi, Enikő Sólyom, András Tóth, Anna Kékesi, Erika P. Tardy, Éva Borbás, Teofil Rétfalvi, Ákos Kiss, and Anikó Korcsmáros

8 Hernando, C., Carrera, M., Ribas, I. és mtsai: Prenatal and postnatal characterization of Y chromosome structural anomalies by molecular cytogenetic analysis. Prenat. Diagn

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Acta Veterinaria Hungarica
Authors: Renáta Fábián, András Kovács, Viktor Stéger, Krisztián Frank, István Egerszegi, János Oláh, and Szilárd Bodó

. A-qin , C. , Zi-rong , X. and Song-dong , Y. ( 2007 ): Sexing goat embryos by PCR amplification of Xand Y-chromosome specific sequence of the amelogenin gene . Asian-Aust. J. Anim. Sci. 20 , 1689 – 1693

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Orvosi Hetilap
Authors: László Ságodi, Janka Jakab, Ákos Kiss, Erzsébet Ladányi, Erzsébet Balogh, Anikó Ujfalusi, Judit Papp, Tímea Megyeri, and Judit Kovács

al.: Phenotypic spectrum of 45,X/46,XY males with a ring Y chromosome and bilaterally descended testes. Fertil. Steril., 2009, 91 , 791–797. Clark A. D. Phenotypic spectrum of 45

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Hematológia–Transzfuziológia
Authors: Nóra Meggyesi, Hajnalka Andrikovics, András Kozma, András Bors, Lívia Varga, Zoltán Őrfi, László Gopcsa, Melinda Paksi, Éva Torbágyi, Nóra Lovas, Marienn Réti, Gergely Kriván, István Vályi-Nagy, and Péter Reményi

al.: Molecular genetic evidence of Y chromosome loss in male patients with hematological disorders. Chinese Medical Journal 2007; 120(22): 2002–2005. 5

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Hematológia–Transzfuziológia
Authors: András Kozma, Melinda Paksi, Emma Ádám, András Bors, Hajnalka Andrikovics, and Gábor Mikala

al. Clinical and biological significance of isolated Y chromosome loss in myelodysplastic syndromes and chronic myelomonocytic leukemia. A report from the Spanish MDS Group. Leuk Res. 2017

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Orvosi Hetilap
Authors: Éva Pinti, Anna Lengyel, Ágnes Sallai, György Fekete, and Irén Haltrich

rendellenességei. In: Szülészeti és Nőgyógyászati Útmutató.] Medition Kiadó, Budapest, 2008; p. 3. [Hungarian] 14 Haltrich I. Phenotypic-genotypic correlations of the Y chromosome

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Acta Veterinaria Hungarica
Authors: S. Bodó, B. Baranyai, Elen Gócza, J. Dohy, and Merja Markkula

. Bradbury , M. W. , Isola , L. M. and Gordon , J. W. ( 1990 ): Enzymatic amplification of a Y chromosome repeat in a single blastomere allows identification of the sex of preimplantation mouse embryos . Proc. Natl. Acad. Sci. USA 87 , 4053 – 4057

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Orvosi Hetilap
Authors: Anna Dávid, Henriett Butz, Zita Halász, Dóra Török, Gábor Nyirő, Ágota Muzsnai, Violetta Csákváry, Andrea Luczay, Ágnes Sallai, Éva Hosszú, Enikő Felszeghy, Attila Tar, Zsuzsanna Szántó, Gy. László Fekete, Imre Kun, Attila Patócs, and Rita Bertalan

Valetto A, Bertini V, Michelucci A, et al. Short stature in isodicentric Y chromosome and three copies of the SHOX gene: clinical report and review of literature. Mol Syndromol. 2016; 7: 19

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Orvosi Hetilap
Authors: Attila Mokánszki, Anikó Ujfalusi, Erzsébet Balogh, Zsuzsanna Molnár, Tamás Sápy, Attila Jakab, Attila Varga, and Éva Oláh

Krausz, C., Rajpert-De Meyts, E., Frydelund-Larsen, L., et al.: Double-blind Y chromosome microdeletion analysis in men with known sperm parameters and reproductive hormone profiles: microdeletions are specific for spermatogenic failure. J. Clin

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