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Institut für Humangenetik

Klinikum / Johannes Gutenberg-Universität Mainz

Publikationen
Ergebnisse pro Seite:  10

Tan, Xiaoying; Xu, Xingbo; Elkenani, Manar et al.

Zfp819, a novel KRAB-zinc finger protein, interacts with KAP1 and functions in genomic integrity maintenance of mouse embryonic stem cells

STEM CELL RESEARCH. Bd. 11. H. 3. 2013 S. 1045-1059


Bartsch, O; Schindler, D; Beyer, V et al.

A girl with an atypical form of ataxia telangiectasia and an additional de novo 3.14 Mb microduplication in region 19q12

EUROPEAN JOURNAL OF MEDICAL GENETICS. Bd. 55. H. 1. 2012 S. 49-55


Karbach, Julia; Coerdt, Wiltrud; Wagner, Wilfried et al.

Case Report: Noonan Syndrome With Multiple Giant Cell Lesions and Review of the Literature

AMERICAN JOURNAL OF MEDICAL GENETICS PART A. Bd. 158A. H. 9. 2012 S. 2283-2289


Schmeh, I; Ziesel, B; Schwind, M et al.

Dunndarmvolvulus infolge eines mesenterialen zystischen Lymphangioms beim Neugeborenen [Abstract]

Monatsschr Kinderheilkd. Bd. 160. H. Spl1. 2012 S. 175


Papaspyrou, K; Mewes, T; Rossmann, H et al.

Head and neck paragangliomas: Report of 175 patients (1989-2010)

HEAD AND NECK-JOURNAL FOR THE SCIENCES AND SPECIALTIES OF THE HEAD AND NECK. Bd. 34. H. 5. 2012 S. 632-637


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