The pericentromeric region of human chromosome 11: evidence for a chromosome-specific duplication.

Intrachromosomal genomic instability in human sporadic colorectal cancer measured by genome-wide allelotyping and inter-(simple sequence repeat) PCR.

Mapping of genes and transcribed sequences in a gene rich 400-kb region on human chromosome 11p15.1-->p14.

Comparative structure, proximal promoter elements, and chromosome location of the human eosinophil major basic protein genes.

p16 (cdkN2/MTS1/INK4A) expression in sporadic colorectal carcinomas.

Spermatid-specific expression of the novel X-linked gene product SPAN-X localized to the nucleus of human spermatozoa.

Assignment of ubiquilin2 (UBQLN2) to human chromosome xp11. 23-->p11.1 by GeneBridge radiation hybrids.

MAGOH interacts with a novel RNA-binding protein.

Genome-wide allelotyping indicates increased loss of heterozygosity on 9p and 14q in early age of onset colorectal cancer.

Assignment of TLL1 and TLL2, which encode human BMP-1/Tolloid-related metalloproteases, to chromosomes 4q32-->q33 and 10q23-->q24 and assignment of murine Tll2 to chromosome 19.

A maternally methylated CpG island in KvLQT1 is associated with an antisense paternal transcript and loss of imprinting in Beckwith-Wiedemann syndrome.

Bestrophin gene mutations in patients with Best vitelliform macular dystrophy.

Structure and chromosomal localization of the human and murine genes for the macrophage MARCO receptor.

The imprinted domain in mouse distal Chromosome 7: reagents for mutagenesis and sequencing.

A model system to study genomic imprinting of human genes.

Mapping, genomic organization and promoter analysis of the human prostate-specific membrane antigen gene.

Coding sequence and expression patterns of mouse chordin and mapping of the cognate mouse chrd and human CHRD genes.

NUP98-HOXD13 gene fusion in therapy-related acute myelogenous leukemia.

Transcript mapping of the human chromosome 11q12-q13.1 gene-rich region identifies several newly described conserved genes.

Promoter sequence, expression, and fine chromosomal mapping of the human gene (MLP) encoding the MARCKS-like protein: identification of neighboring and linked polymorphic loci for MLP and MACS and use in the evaluation of human neural tube defects.