M. Ross

发表

Sequence analysis and transcript identification within 1.5 MB of DNA deleted together with the NDP and MAO genes in atypical Norrie disease patients presenting with a profound phenotype

J. Bye, I. Craig, B. Suárez-Merino, 2001, Human mutation.

Deletion mapping on chromosome 10p and definition of a critical region for the second DiGeorge syndrome locus (DGS2)

T. Meitinger, S. Schuffenhauer, P. Lichtner, 1998, European Journal of Human Genetics.

Translocation between chromosomes 6 and 15 (45,XX,t(6;15)(q25;q11.2)) with further evidence for lack of imprinting of the insulin-like growth factor II/mannose-6-phosphate receptor in humans.

C. Polychronakos, M. Vekemans, V. D. Der Kaloustian, 1996, Journal of medical genetics.

UHX1 and PCTK1: precise characterisation and localisation within a gene-rich region in Xp11.23 and evaluation as candidate genes for retinal diseases mapped to Xp21.1–p11.2

A. Rosenthal, M. Platzer, G. Nyakatura, 1998, European Journal of Human Genetics.

Long-range map of a 3.5-Mb region in Xp11.23-22 with a sequence-ready map from a 1.1-Mb gene-rich interval.

T. Meitinger, A. Meindl, H. Hellebrand, 1996, Genome research.

Human methionine synthase: cDNA cloning and identification of mutations in patients of the cblG complementation group of folate/cobalamin disorders.

P. Goyette, R. Rozen, P. Goyette, 1996, Human molecular genetics.

A novel poly(A)-binding protein gene (PABPC5) maps to an X-specific subinterval in the Xq21.3/Yp11.2 homology block of the human sex chromosomes.

G. Howell, M. Ross, N. Affara, 2001, Genomics.

Physical and transcriptional mapping of the X-linked cleft palate and ankyloglossia (CPX) critical region

G. Howell, P. Stanier, M. Ross, 2001, Human Genetics.

A gene (SRPX) encoding a sushi-repeat-containing protein is deleted in patients with X-linked retinitis pigmentosa.

T. Meitinger, B. Lorenz, A. Meindl, 1995, Human molecular genetics.

Advances in Brief DNA Strand Break Rejoining Defect in xrs-6 Is Complemented by Transfection with the Human Ku 80 Gene 1

Natasha, Gillian, P. Jeggo, 2006 .

Identification and characterization of the human homologue (RAI2) of a mouse retinoic acid-induced gene in Xp22.

P. Sieving, M. Ross, M. Vaudin, 1999, Genomics.

Positional Cloning in Xp 22 : towards the isolation of the gene involved in X-linked retinoschisis

W. Wagenaar, R. Pavitt, J. T. Dunnen, 2014 .

The t(X;1)(p11.2;q21.2) translocation in papillary renal cell carcinoma fuses a novel gene PRCC to the TFE3 transcription factor gene.

S Gill, R. Gwilliam, C. Cooper, 1996, Human molecular genetics.