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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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. Mende— P. Langó— K. Csete— A. Zsolnai— E. K. Conant— C. S. Downes— I. Raskó : Y-chromosome analysis of ancient Hungarian and two modern Hungarian-speaking populations from the Carpathian basin. Annhumgen 72 (2008 July) 519

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, P., Ibrahim, M., Jenkins, T., Kidd, J. R., Qasim Mehdi, S., Seielstad, M. T., Wells, R. S., Piazza, A., Davis, R. W., Feldman, M. W., Cavalli-Sforza, L. L. and Oefner, P. J. (2000): Y chromosome sequence variation and the history of human populations

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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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of Haplogroup G1 Provides Estimates of SNP and STR Mutation Rates on the Human Y Chromosome and Reveals Migrations of Iranic Speakers . PLoS One Vol. 10 , No. 4 : e0122968 . doi.org/10.1371/journal.pone.0122968

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Acta Biologica Hungarica
Authors: Edit Nádasi, P. Gyűrűs, Márta Czakó, Judit Bene, Sz. Kosztolányi, Sz. Fazekas, P. Dömösi, and B. Melegh

Lahermo, P., Savontaus, M.-L., Sistonen, P., Beres, J., de Knijff, P., Aula, P., Sajantila, A. (1999) Y chromosomal polymorphisms reveal founding lineages in the Finns and the Saami. Eur. J. Hum. Genet. 7 , 447

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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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