G. von Beust

发表

Molecular cloning, expression and chromosome location of the human pelota gene PELO

I. Adham, W. Engel, R. Shamsadin, 2000, Cytogenetic and Genome Research.

Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter → p12.2)[10]

T. Liehr, B. Zoll, P. Burfeind, 2003, American journal of medical genetics. Part A.

Molecular cloning, chromosomal localization, and expression analysis of CYRN1 and CYRN2, two human genes coding for cyritestin, a sperm protein involved in gamete interaction.

M. Mattei, I. Adham, W. Engel, 1998, DNA and cell biology.

Analysis of the Origin of the Extra Chromosome in Trisomy 8 in 4 Cases of Spontaneous Abortions

G. Karadima, D. Vassilopoulos, K. Brøndum‐Nielsen, 1998, Fetal Diagnosis and Therapy.

Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay

T. Liehr, B. Zoll, P. Burfeind, 2005, American journal of medical genetics. Part A.

DNA analysis of Huntington’s disease

O. Riess, C. Zühlke, G. von Beust, 1999, Neurology.

Assignment of the human melanoma inhibitory activity gene (MIA) to 19q13.32-q13.33 by fluorescence in situ hybridization (FISH).

A. Bosserhoff, M. Schmid, U. Bogdahn, 1996, Genomics.

Prenatal Diagnosis and Fetopathological Findings in a Fetus with Ring Chromosome 18

H. Rehder, B. Zoll, I. Hansmann, 1998, Fetal Diagnosis and Therapy.

Extra Euchromatic Band in the qh Region of Chromosome 9

K. Bink, G. von Beust, 1999, Fetal Diagnosis and Therapy.

Origin of nondisjunction in trisomy 8 and trisomy 8 mosaicism

E. Blennow, S. Kitsiou‐Tzeli, A. Tsezou, 1998, European Journal of Human Genetics.