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Institut für Humangenetik

Klinikum / Johannes Gutenberg-Universität Mainz

Publikationen
Ergebnisse pro Seite:  25

Mikelsaar, R; Molder, H; Bartsch, O et al.

Two novel deletions (array CGH findings) in pigment dispersion syndrome.

Ophthalmic Genet. Bd. 28. H. 4. 2007 S. 216-9


Yue, Y; Haaf, T

7E olfactory receptor gene clusters and evolutionary chromosome rearrangements

Cytogenet Genome Res. Bd. 112. 2006 S. 6-10


Metzler, M; Forster, A; Pannell, R et al.

A conditional model of MLL-AF4 B-cell tumourigenesis using invertor technology.

Oncogene. Bd. 25. H. 22. 2006 S. 3093-103



Garcia, NM; Allgood, J; Santos, LJ et al.

DELETION MAPPING OF CRITICAL REGION FOR HYPOSPADIAS, PENOSCROTAL TRANSPOSITION AND IMPERFORATE ANUS ON HUMAN CHROMOSOME 13.

J Pediatr Urol. Bd. 2. H. 4. 2006 S. 233-242






Ruf, N; Dünzinger, U; Brinckmann, A et al.

Expression profiling of uniparental mouse embryos is inefficient in identifying novel imprinted genes

Genomics. Bd. 87. 2006 S. 509-519


Haaf, T

Fine mapping of gene ordering by elongated chromosome methods

Celis J (Hrsg). Cell Biology: A Laboratory Handbook. Volume 3. 3. Aufl. The Netherlands: Elsvier 2006


Schneider, G; Weber, A; Zechner, U et al.

GADD45alpha is highly expressed in pancreatic ductal adenocarcinoma cells and required for tumor cell viability.

Int J Cancer. Bd. 118. H. 10. 2006 S. 2405-11


Loitzsch, A; Bartsch, O

Healthy 12-year-old boy with mosaic inv dup(15)(q13).

Am J Med Genet. Bd. 140. H. 6. 2006 S. 640-3


Nayernia, K; Nolte, J; Michelmann, HW et al.

In vitro-differentiated embryonic stem cells give rise to male gametes that can generate offspring mice

Dev Cell. Bd. 11. 2006 S. 125-132


Daser, A; Thangavelu, M; Pannell, R et al.

Interrogation of genomes by molecular copy-number counting (MCC)

Nat Methods. Bd. 3. 2006 S. 447-453


Yue, Y; Grossmann, B; Galetzka, D et al.

Isolation and differential expression of two isoforms of ROBO2/Robo2 axon guidance receptor gene in humans and mice

Genomics. Bd. 88. 2006 S. 772-778


El-Maarri, O; Singer, H; Klein, C et al.

Lack of F8 mRNA: a novel mechanism leading to hemophilia A

Blood. Bd. 107. 2006 S. 2759-2765


Haaf, T

Methylation dynamics in the early mammalian embryo: implications of genome reprogramming defects for development

Doerfler W, Boehm P (Hrsg). Current Topics in Microbiology and Immunology. 310. Aufl. Berlin: Springer 2006


Fauth, C; Gribble, SM; Porter, KM et al.

Micro-array analyses decipher exceptional complex familial chromosomal rearrangement

Hum Genet. Bd. 119. 2006 S. 145-153


Bartsch, O; Seemanova, E

Microdeletion Syndromes

Ganten D, Ruckpaul K (Hrsg). Encyclopedic Reference of Genomics and Proteomics in Molecular Medicine. 1. Aufl. Berlin, Heidelberg, New York: Springer 2006


Oiglane-Shlik, E; Talvik, T; Zordania, R et al.

Prevalence of Angelman syndrome and Prader-Willi syndrome in Estonian children: sister syndromes not equally represented.

Am J Med Genet. Bd. 140. H. 18. 2006 S. 1936-43


Yue, Y; Tsend-Ayush, E; Grützner, F et al.

Segmental duplication associated with evolutionary instability of human chromosome 3p25.1

Cytogenet Genome Res. Bd. 112. 2006 S. 202-207


Nijnik, A; Ferry, H; Lewis, G et al.

Spontaneous B cell hyperactivity in autoimmune-prone MRL mice.

Int Immunol. Bd. 18. H. 7. 2006 S. 1127-37


Eggermann, T; Krause-Plonka, I; Wollmann, HA et al.

Supernumerary marker chromosome 7 and maternal uniparental disomy 7 in a boy with growth retardation and triangular face.

Clin Dysmorphol. Bd. 15. H. 1. 2006 S. 9-12


Oiglane-Shlik, E; Zordania, R; Varendi, H et al.

The neonatal phenotype of Prader-Willi syndrome.

Am J Med Genet. Bd. 140. H. 11. 2006 S. 1241-4