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1
Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma
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Hearing impairment locus heterogeneity and identification of PLS1 as a new autosomal dominant gene in Hungarian Roma

Schrauwen, Isabelle ; Melegh, Béla I ; Chakchouk, Imen ; Acharya, Anushree ; Nasir, Abdul ; Poston, Alexis ; Cornejo-Sanchez, Diana M ; Szabo, Zsolt ; Karosi, Tamás ; Bene, Judit ; Melegh, Béla ; Leal, Suzanne M

European journal of human genetics : EJHG, 2019-06, Vol.27 (6), p.869-878 [Periódico revisado por pares]

England: Nature Publishing Group

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2
Genome-wide autosomal, mtDNA, and Y chromosome analysis of King Bela III of the Hungarian Arpad dynasty
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Artigo
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Genome-wide autosomal, mtDNA, and Y chromosome analysis of King Bela III of the Hungarian Arpad dynasty

Wang, Chuan-Chao ; Posth, Cosimo ; Furtwängler, Anja ; Sümegi, Katalin ; Bánfai, Zsolt ; Kásler, Miklós ; Krause, Johannes ; Melegh, Béla

Scientific reports, 2021-09, Vol.11 (1), p.19210-19210, Article 19210 [Periódico revisado por pares]

England: Nature Publishing Group

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3
Characterization of Danube Swabian population samples on a high-resolution genome-wide basis
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Artigo
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Characterization of Danube Swabian population samples on a high-resolution genome-wide basis

Bánfai, Zsolt ; Kövesdi, Erzsébet ; Sümegi, Katalin ; Büki, Gergely ; Szabó, András ; Magyari, Lili ; Ádám, Valerián ; Pálos, Ferenc ; Miseta, Attila ; Kásler, Miklós ; Melegh, Béla

BMC genomics, 2023-01, Vol.24 (1), p.9-9, Article 9 [Periódico revisado por pares]

England: BioMed Central Ltd

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4
Author Correction: Genome-wide autosomal, mtDNA, and Y chromosome analysis of King Bela III of the Hungarian Arpad dynasty
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Artigo
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Author Correction: Genome-wide autosomal, mtDNA, and Y chromosome analysis of King Bela III of the Hungarian Arpad dynasty

Wang, Chuan-Chao ; Posth, Cosimo ; Furtwängler, Anja ; Sümegi, Katalin ; Bánfai, Zsolt ; Kásler, Miklós ; Krause, Johannes ; Melegh, Béla

Scientific reports, 2022-05, Vol.12 (1), p.7157-7157, Article 7157 [Periódico revisado por pares]

England: Nature Publishing Group

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5
Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report
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Artigo
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Novel phenotypic variant in the MYH7 spectrum due to a stop-loss mutation in the C-terminal region: a case report

Bánfai, Zsolt ; Hadzsiev, Kinga ; Pál, Endre ; Komlósi, Katalin ; Melegh, Márton ; Balikó, László ; Melegh, Béla

BMC medical genetics, 2017-09, Vol.18 (1), p.105-105, Article 105 [Periódico revisado por pares]

England: BioMed Central Ltd

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6
Genotype-Phenotype Associations in Patients With Type-1, Type-2, and Atypical NF1 Microdeletions
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Artigo
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Genotype-Phenotype Associations in Patients With Type-1, Type-2, and Atypical NF1 Microdeletions

Büki, Gergely ; Zsigmond, Anna ; Czakó, Márta ; Szalai, Renáta ; Antal, Gréta ; Farkas, Viktor ; Fekete, György ; Nagy, Dóra ; Széll, Márta ; Tihanyi, Marianna ; Melegh, Béla ; Hadzsiev, Kinga ; Bene, Judit

Frontiers in genetics, 2021-06, Vol.12, p.673025-673025 [Periódico revisado por pares]

Frontiers Media S.A

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7
Reply to Letter by Tellier et al., 'Scientific refutation of ESHG statement on embryo selection'
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Reply to Letter by Tellier et al., 'Scientific refutation of ESHG statement on embryo selection'

Forzano, Francesca ; Antonova, Olga ; Clarke, Angus ; de Wert, Guido ; Hentze, Sabine ; Jamshidi, Yalda ; Moreau, Yves ; Perola, Markus ; Prokopenko, Inga ; Read, Andrew ; Reymond, Alexandre ; Stefansdottir, Vigdis ; van El, Carla ; Genuardi, Maurizio

European journal of human genetics : EJHG, 2023-03, Vol.31 (3), p.279-281 [Periódico revisado por pares]

England: Nature Publishing Group

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8
Genome-Wide Marker Data-Based Comparative Population Analysis of Szeklers From Korond, Transylvania, and From Transylvania Living Non-Szekler Hungarians
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Genome-Wide Marker Data-Based Comparative Population Analysis of Szeklers From Korond, Transylvania, and From Transylvania Living Non-Szekler Hungarians

Ádám, Valerián ; Bánfai, Zsolt ; Sümegi, Katalin ; Büki, Gergely ; Szabó, András ; Magyari, Lili ; Miseta, Attila ; Kásler, Miklós ; Melegh, Béla

Frontiers in genetics, 2022-03, Vol.13, p.841769-841769 [Periódico revisado por pares]

Switzerland: Frontiers Media S.A

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9
Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy
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Artigo
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Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy

Alonso-Pérez, Jorge ; González-Quereda, Lidia ; Bruno, Claudio ; Panicucci, Chiara ; Alavi, Afagh ; Nafissi, Shahriar ; Nilipour, Yalda ; Zanoteli, Edmar ; Isihi, Lucas Michielon de Augusto ; Melegh, Béla ; Hadzsiev, Kinga ; Muelas, Nuria ; Vílchez, Juan J ; Dourado, Mario Emilio ; Kadem, Naz ; Kutluk, Gultekin ; Umair, Muhammad ; Younus, Muhammad ; Pegorano, Elena ; Bello, Luca ; Crawford, Thomas O ; Suárez-Calvet, Xavier ; Töpf, Ana ; Guglieri, Michela ; Marini-Bettolo, Chiara ; Gallano, Pia ; Straub, Volker ; Díaz-Manera, Jordi

Brain (London, England : 1878), 2022-04, Vol.145 (2), p.596-606 [Periódico revisado por pares]

England: Oxford University Press

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10
Genetic structure of Europeans: a view from the North-East
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Artigo
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Genetic structure of Europeans: a view from the North-East

Nelis, Mari ; Esko, Tõnu ; Mägi, Reedik ; Zimprich, Fritz ; Zimprich, Alexander ; Toncheva, Draga ; Karachanak, Sena ; Piskácková, Tereza ; Balascák, Ivan ; Peltonen, Leena ; Jakkula, Eveliina ; Rehnström, Karola ; Lathrop, Mark ; Heath, Simon ; Galan, Pilar ; Schreiber, Stefan ; Meitinger, Thomas ; Pfeufer, Arne ; Wichmann, H-Erich ; Melegh, Béla ; Polgár, Noémi ; Toniolo, Daniela ; Gasparini, Paolo ; D'Adamo, Pio ; Klovins, Janis ; Nikitina-Zake, Liene ; Kucinskas, Vaidutis ; Kasnauskiene, Jūrate ; Lubinski, Jan ; Debniak, Tadeusz ; Limborska, Svetlana ; Khrunin, Andrey ; Estivill, Xavier ; Rabionet, Raquel ; Marsal, Sara ; Julià, Antonio ; Antonarakis, Stylianos E ; Deutsch, Samuel ; Borel, Christelle ; Attar, Homa ; Gagnebin, Maryline ; Macek, Milan ; Krawczak, Michael ; Remm, Maido ; Metspalu, Andres Fleischer, Robert C.

PloS one, 2009-05, Vol.4 (5), p.e5472-e5472 [Periódico revisado por pares]

United States: Public Library of Science

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