A. Mertz

发表

Characterization of a YAC contig spanning the pseudoautosomal region.

J. Ellison, J. Riley, H. Lehrach, 1995, Genomics.

FISH localization of the human Y-homolog of protein kinase PRKX (PRKY) to Yp11.2 and two pseudogenes to 15q26 and Xq12-->q13.

G. Rappold, W. Schempp, B. Gläser, 1997, Cytogenetics and cell genetics.

Assignment of a human homolog of the mouse Htr3 receptor gene to chromosome 11q23.1-q23.2.

E. Schröck, G. Rappold, B. Weiss, 1995, Genomics.

Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome

A. Rosenthal, A. Rump, G. Nordsiek, 1997, Nature Genetics.

Abnormal XY interchange between a novel isolated protein kinase gene, PRKY, and its homologue, PRKX, accounts for one third of all (Y+)XX males and (Y-)XY females.

D. Page, C. Petit, D. Weil, 1997, Human molecular genetics.

Molecular studies of an X;Y translocation chromosome in a woman with deletion of the pseudoautosomal region but normal height

S. Kirsch, S. Spranger, K. Schiebel, 1997, Clinical genetics.

FISH-deletion mapping defines a 270-kb short stature critical interval in the pseudoautosomal region PAR1 on human sex chromosomes

G. Rappold, T. Ogata, E. Rao, 1997, Human Genetics.

A resource of targeted mutant mouse lines for 5,061 genes

Steve D. M. Brown, Diana L. Young, Jennie R. Green, 2019, bioRxiv.

Aneuploidy screening of embryonic stem cell clones by metaphase karyotyping and droplet digital polymerase chain reaction

Y. Hérault, J. Mianné, L. Teboul, 2016, BMC Cell Biology.

A resource of targeted mutant mouse lines for 5,061 genes

Diana L. Young, Jennie R. Green, Juan J. Gallegos, 2021, Nature Genetics.