T. J. Wright

发表

High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome.

E. Haan, G. Sutherland, O. Riess, 1997, American journal of medical genetics.

Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Hirschhorn syndrome.

A. Battaglia, R. Tenconi, G. Neri, 2000, American journal of medical genetics.

Wolf-Hirschhorn (4p-) syndrome.

A. Battaglia, J. Carey, T. J. Wright, 2005, Advances in pediatrics.

Comparative analysis of a novel gene from the Wolf-Hirschhorn/Pitt-Rogers-Danks syndrome critical region.

M. Altherr, P. Francis-West, C. Naranjo, 1999, Genomics.

WHSC1, a 90 kb SET domain-containing gene, expressed in early development and homologous to a Drosophila dysmorphy gene maps in the Wolf-Hirschhorn syndrome critical region and is fused to IgH in t(4;14) multiple myeloma.

A. Moorman, P. D. de Boer, J. T. Dunnen, 1998, Human molecular genetics.

Wolf-Hirschhorn and Pitt-Rogers-Danks syndromes caused by overlapping 4p deletions.

M. Altherr, O. Quarrell, M. Clemens, 1998, American journal of medical genetics.

Delimiting the Wolf-Hirschhorn syndrome critical region to 750 kilobase pairs.

V. P. Johnson, M. Altherr, A. V. Perez-Castro, 1997, American journal of medical genetics.

A transcript map of the newly defined 165 kb Wolf-Hirschhorn syndrome critical region.

E. Zackai, N. Spinner, K. Hirschhorn, 1997, Human molecular genetics.

Identification of the first gene (FRG1) from the FSHD region on human chromosome 4q35.

J E Hewitt, R. Frants, J. Hewitt, 1996, Human molecular genetics.

The FSHD-associated repeat, D4Z4, is a member of a dispersed family of homeobox-containing repeats, subsets of which are clustered on the short arms of the acrocentric chromosomes.

R. Lyle, L. Clark, J. Hewitt, 1995, Genomics.

Search for the FSHD gene using cDNA selection in a region spanning 100 kb on chromosome 4q35

C. Wijmenga, J. Rommens, R. Frants, 1995, Muscle & nerve. Supplement.

Analysis of the tandem repeat locus D4Z4 associated with facioscapulohumeral muscular dystrophy.

J E Hewitt, C. Wijmenga, R. Lyle, 1994, Human molecular genetics.

Physical mapping and YAC-cloning connects four genetically distinct 4qter loci (D4S163, D4S139, D4F35S1 and D4F104S1) in the FSHD gene-region.

C. Wijmenga, R. Williamson, J. Hewitt, 1993, Human molecular genetics.

Fine mapping of the FSHD gene region orientates the rearranged fragment detected by the probe p13E-11.

C. Wijmenga, R. Williamson, L. Clark, 1993, Human molecular genetics.

Chromosome 4q DNA rearrangements associated with facioscapulohumeral muscular dystrophy

C. Wijmenga, G. van Ommen, R. Williamson, 1992, Nature genetics.

Reply to the letter to the editor by Partington and Turner—“Wolf-Hirschhorn and Pitt-Rogers-Danks syndromes”

K. Hirschhorn, D. Callen, M. Altherr, 1999 .

"Tandem" duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotype.

M. Altherr, M. Zollino, C. Di Stefano, 1999, American journal of medical genetics.

Molecular genetics of facioscapulohumeral muscular dystrophy

C. Wijmenga, R. Frants, J. Hewitt, 1993, Neuromuscular Disorders.