Maternal uniparental disomy 7 : review and further delineation of the phenotype
KOTZOT, D, BALMER, D, TARIVERDIAN, G, SCHINZEL, A, BAUMER, A, CHRZANOWSKA, K, HAMEL, B. C. J, ILYINA, H, KRAJEWSKA-WALASEK, M, LURIE, I. W, OTTEN, B. J, SCHOENLE, E
Published in European journal of pediatrics (01.04.2000)
Published in European journal of pediatrics (01.04.2000)
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Agnathia-otocephaly complex: presentation of four cases
Schiffer, C., Tariverdian, G., Schiesser, M., Sergi, C.
Published in Pathology, research and practice (01.01.2004)
Published in Pathology, research and practice (01.01.2004)
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Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation
Jensen, Lars Riff, Amende, Marion, Gurok, Ulf, Moser, Bettina, Gimmel, Verena, Tzschach, Andreas, Janecke, Andreas R., Tariverdian, Gholamali, Chelly, Jamel, Fryns, Jean-Pierre, Van Esch, Hilde, Kleefstra, Tjitske, Hamel, Ben, Moraine, Claude, Gécz, Jozef, Turner, Gillian, Reinhardt, Richard, Kalscheuer, Vera M., Ropers, Hans-Hilger, Lenzner, Steffen
Published in American journal of human genetics (01.02.2005)
Published in American journal of human genetics (01.02.2005)
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Molecular analysis of aniridia patients for deletions involving the Wilms' tumor gene
Drechsler, M, Meijers-Heijboer, E J, Schneider, S, Schurich, B, Grond-Ginsbach, C, Tariverdian, G, Kantner, G, Blankenagel, A, Kaps, D, Schroeder-Kurth, T
Published in Human genetics (01.10.1994)
Published in Human genetics (01.10.1994)
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Wolf-Hirschhorn syndrome: case report and review of the chromosomal aberrations associated with diaphragmatic defects
Sergi, C, Schulze, B R, Hager, H D, Beedgen, B, Zilow, E, Linderkamp, O, Otto, H F, Tariverdian, G
Published in Pathologica (01.06.1998)
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Published in Pathologica (01.06.1998)
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The Novel Rho-GTPase Activating Gene MEGAP/srGAP3 Has a Putative Role in Severe Mental Retardation
Endris, Volker, Wogatzky, Birgit, Leimer, Uwe, Bartsch, Dusan, Zatyka, Malgorzata, Latif, Farida, Maher, Eamonn R., Tariverdian, Gholamali, Kirsch, Stefan, Karch, Dieter, Rappold, Gudrun A.
Published in Proceedings of the National Academy of Sciences - PNAS (03.09.2002)
Published in Proceedings of the National Academy of Sciences - PNAS (03.09.2002)
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Molecular analysis of mutations in the gene FMR-1 segregating in fragile X families
Steinbach, P, Wöhrle, D, Tariverdian, G, Kennerknecht, I, Barbi, G, Edlinger, H, Enders, H, Götz-Sothmann, M, Heilbronner, H, Hosenfeld, D
Published in Human genetics (01.11.1993)
Published in Human genetics (01.11.1993)
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Allelic heterogeneity in the COH1 gene explains clinical variability in Cohen syndrome
HENNIES, Hans Christian, RAUCH, Anita, GIUGLIANI, Roberto, NEUMANN, Thomas E, ECKL, Katja M, KARBASIYAN, Mohsen, REIS, André, HORN, Denise, SEIFERT, Wenke, SCHUMI, Christian, MOSER, Elisabeth, AL-TAJI, Eva, TARIVERDIAN, Gholamali, CHRZANOWSKA, Krystyna H, KRAJEWSKA-WALASEK, Malgorzata, RAJAB, Anna
Published in American journal of human genetics (01.07.2004)
Published in American journal of human genetics (01.07.2004)
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Mental retardation, acromegalic face, and megalotestes in two half-brothers: a specific form of X-linked mental retardation without fra(X) (q)?
Tariverdian, G, Froster-Iskenius, U, Deuschl, G, Wolff, G
Published in American journal of medical genetics (01.02.1991)
Published in American journal of medical genetics (01.02.1991)
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Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses
RIESEWIJK, A. M, HU, L, SCHULZ, U, TARIVERDIAN, G, HÖGLUND, P, KERE, J, ROPERS, H.-H, KALSCHEUER, V. M
Published in Genomics (San Diego, Calif.) (01.06.1997)
Published in Genomics (San Diego, Calif.) (01.06.1997)
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