Martina Broghammer

发表

Intrapopulational relationships in ancient societies: a multidisciplinary study.

C. Pusch, M. Scholz, S. Hengst, 2001, Zeitschrift fur Morphologie und Anthropologie.

Internal Alu-polymerase chain reaction: a sensitive contamination monitoring protocol for DNA extracted from prehistoric animal bones.

L. Bachmann, C. Pusch, M. Scholz, 2000, Analytical biochemistry.

Voltage‐induced release of nucleic acids from palaeontological samples

I. Giddings, L. Bachmann, C. Pusch, 2000, Electrophoresis.

PCR-induced sequence alterations hamper the typing of prehistoric bone samples for diagnostic achondroplasia mutations.

L. Bachmann, A. Nerlich, I. Kennerknecht, 2004, Molecular biology and evolution.

CNGA3 mutations in hereditary cone photoreceptor disorders.

S. Jacobson, R. Salati, L. Sharpe, 2001, American journal of human genetics.

Molecular phylogenetics employing modern and ancient DNA.

C. Pusch, N. Blin, Martina Broghammer, 2003, Journal of applied genetics.

Refinement of the MYP3 locus on human chromosome 12 in a German family with Mendelian autosomal dominant high-grade myopia by SNP array mapping.

U. Stephani, G. Nürnberg, C. Becker, 2008, International journal of molecular medicine.

Review A genetic perspective on myopia

C. Pusch, Martina Broghammer, F. Jacobi, 2005 .

A genetic perspective on myopia

E. Zrenner, C. Pusch, Martina Broghammer, 2005, Cellular and Molecular Life Sciences CMLS.

A novel CACNA1F mutation in a french family with the incomplete type of X-linked congenital stationary night blindness.

C. Pusch, N. Blin, Martina Broghammer, 2003, American journal of ophthalmology.

Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina

A. Chapelle, B. Lorenz, E. Zrenner, 2002, European Journal of Human Genetics.

Mutations in the CNGB3 gene encoding the beta-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia (ACHM3) linked to chromosome 8q21.

P. Sieving, L. Sharpe, E. Zrenner, 2000, Human molecular genetics.

Mutations in the CNGB 3 gene encoding the β-subunit of the cone photoreceptor cGMP-gated channel are responsible for achromatopsia ( ACHM 3 ) linked to chromosome 8 q 21

P. Sieving, L. Sharpe, E. Zrenner, 2000 .

Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11.

S. Jacobson, L. Sharpe, E. Zrenner, 1998, Genomics.

Ten novel ORF15 mutations confirm mutational hot spot in the RPGR gene in European patients with X‐linked retinitis pigmentosa

B. Jurklies, D. Besch, C. Pusch, 2002, Human mutation.

Population Haplotypes of Exon ORF15 of the Retinitis Pigmentosa GTPase Regulator Gene in Germany

C. Pusch, N. Blin, Martina Broghammer, 2012, Molecular Diagnosis & Therapy.

Cremation practices and the survival of ancient DNA: burnt bone analyses via RAPD-mediated PCR.

C. Pusch, M. Scholz, Martina Broghammer, 2000, Anthropologischer Anzeiger; Bericht uber die biologisch-anthropologische Literatur.