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Institut für Humangenetik

Klinikum / Johannes Gutenberg-Universität Mainz

Publikationen
Ergebnisse pro Seite:  10

Schneider, E.; Mayer, S.; El Hajj, N. et al.

Methylation and Expression Analyses of the 7q Autism Susceptibility Locus Genes MEST, COPG2, and TSGA14 in Human and Anthropoid Primate Cortices

CYTOGENETIC AND GENOME RESEARCH. Bd. 136. H. 4. 2012 S. 278-287



Galetzka, D; Hansmann, T; El Hajj, N et al.

Monozygotic twins discordant for constitutive BRCA1 promoter methylation, childhood cancer and secondary cancer

EPIGENETICS. Bd. 7. H. 1. 2012 S. 47-54


Bartsch, O; Zechner, U; Kirmes, A et al.

Novel VANGL1 Gene Mutations in 144 Slovakian, Romanian and German

Mol Syndromol 2012. Bd. 3. 2012 S. 76-81


Kidszun, Andre; Fuchs, Anne-Jule; Russo, Alexandra et al.

Skeletal abnormalities of the upper limbs - Neonatal diagnosis of 49,XXXXY syndrome

GENE. Bd. 508. H. 1. 2012 S. 117-120


Siuda, D; Zechner, U; Prawitt, D et al.

Transcriptional regulation of Nox4 by histone deacetylases

NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY. Bd. 385. 2012 S. 91-91


Siuda, D; Zechner, U; El Hajj, N et al.

Transcriptional regulation of Nox4 by histone deacetylases in human endothelial cells

BASIC RESEARCH IN CARDIOLOGY. Bd. 107. H. 5. 2012 S. -



Kim, HG; Kim, HT; Leach, NT et al.

Translocations Disrupting PHF21A in the Potocki-Shaffer-Syndrome Region Are Associated with Intellectual Disability and Craniofacial Anomalies

AMERICAN JOURNAL OF HUMAN GENETICS. Bd. 91. H. 1. 2012 S. 56-72


Caglayan, AO; Lechno, S; Gumus, H et al.

A BOY WITH CLASSICAL RUBINSTEIN-TAYBI SYNDROME BUT NO DETECTABLE MUTATION IN THE CREBBP AND EP300 GENES

GENETIC COUNSELING. Bd. 22. H. 4. 2011 S. 341-346