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Institut für Humangenetik

Klinikum / Johannes Gutenberg-Universität Mainz

Publikationen
Ergebnisse pro Seite:  10

Bartsch, O; Labonte, J; Albrecht, B et al.

Two Patients With EP300 Mutations and Facial Dysmorphism Different From the Classic Rubinstein-Taybi Syndrome

AMERICAN JOURNAL OF MEDICAL GENETICS PART A. Bd. 152A. H. 1. 2010 S. 181-184


Puhl, AG; Zelazny, J; Galetzka, D et al.

Unbalanced translocation 6p/16q (partial monosomy 6p and trisomy 16q): prenatal diagnosis and cytogenetics

EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY. Bd. 150. H. 2. 2010 S. 119-125


Lehnen, H; Schafer, S; Poarangan, C et al.

Unequivocal Determination of Zygosity of Same-Sex Twins by Molecular Genetic Analysis

GEBURTSHILFE UND FRAUENHEILKUNDE. Bd. 70. H. 12. 2010 S. 979-984





Haensel, J; Kohlschmidt, N; Pitz, S et al.

Case Report Supporting That the Barber-Say and Ablepharon Macrostomia Syndromes Could Represent One Disorder

Am J Med Genet. Bd. 149. 2009 S. 2236-2240



Hansmann, T; Nanda, I; Volobouev, V et al.

Cross-Species Chromosome Painting Corroborates Microchromosome Fusion during Karyotype Evolution of Birds

CYTOGENETIC AND GENOME RESEARCH. Bd. 126. H. 3. 2009 S. 281-304


Farcas, R; Schneider, E; Frauenknecht, K et al.

Differences in DNA methylation patterns and expression of the CCRK gene in human and nonhuman primate cortices.

Mol Biol Evol. Bd. 26. H. 6. 2009 S. 1379-89