X. Zhu

发表

Methylenetetrahydrofolate reductase genotypes and haplotypes associated with susceptibility to colorectal cancer in an eastern Chinese Han population.

H. Shen, W. Xu, X. Zhu, 2011, Genetics and molecular research : GMR.

Strong correlation of elastin deletions, detected by FISH, with Williams syndrome: evaluation of 235 patients.

C. Morris, J. Carey, A. Brothman, 1995, American journal of human genetics.

Allelic loss detected on chromosomes 8, 10, and 17 by fluorescence in situ hybridization using single-copy P1 probes on isolated nuclei from paraffin-embedded prostate tumors.

M. Becich, G. Miller, A. Brothman, 1997, The American journal of pathology.

Evaluation of 20 archival prostate tumor specimens by fluorescence in situ hybridization (FISH).

A. Brothman, B. Williams, L. Rohr, 1994, Cancer Genetics and Cytogenetics.

The detection of contiguous gene deletions at the neurofibromatosis 1 locus with fluorescence in situ hybridization.

V. P. Johnson, D. Viskochil, K. Stephens, 1996, Cytogenetics and cell genetics.

Assignment of human xanthine dehydrogenase gene to chromosome 2p22.

A. Brothman, J. Hoidal, T. Huecksteadt, 1994, Genomics.

Evidence for a tumor suppressor gene distal to BRCA1 in prostate cancer.

A. Brothman, R. Stephenson, Michael R. Steele, 1996, The Journal of urology.

Cyclin D1 protein overexpression and gene amplification in benign breast tissue and breast cancer risk

T. Rohan, R. Kandel, S-Q Li, 2001, European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation.

Expansion in size of a terminal deletion: a paradigm shift for parental follow-up studies

S. South, A. Rope, A. Brothman, 2008, Journal of Medical Genetics.

Comparison of targeted and whole genome analysis of postnatal specimens using a commercially available array based comparative genomic hybridisation (aCGH) microarray platform

S. South, A. Brothman, E. Aston, 2008, Journal of Medical Genetics.

Identification of neurofibromatosis 1 (NF1) homologous loci by direct sequencing, fluorescence in situ hybridization, and PCR amplification of somatic cell hybrids.

R. Cawthon, D. Viskochil, Y. Li, 1995, Genomics.

A common deletion at chromosomal region 17q21 in sporadic prostate tumors distal to BRCA1.

A. Brothman, R. Stephenson, J. Cui, 2001, Genomics.

Microdissection, DOP-PCR, and comparative genomic hybridization of paraffin-embedded familial prostate cancers.

M. Skolnick, L. Cannon-Albright, S. Tavtigian, 2000, Cancer genetics and cytogenetics.

Chromosome 7 abnormalities in prostate cancer detected by dual-color fluorescence in situ hybridization.

A. Brothman, J. Cui, L. Rohr, 1998, Cancer genetics and cytogenetics.

Gene identification using exon amplification on human chromosome 18q21: implications for bipolar disorder

M. McInnis, C. Ross, R. Reeves, 2000, Molecular Psychiatry.

Cyclin D1 gene amplification and protein expression in benign breast disease and breast carcinoma.

T. Rohan, R. Kandel, W. Hartwick, 1998, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

Physical and genetic localization of a Shab subfamily potassium channel (KCNB1) gene to chromosomal region 20q13.2.

O. Pongs, A. Brothman, M. Leppert, 1995, Genomics.

Molecular cytogenetic analysis of a t(7;10) in a human glioblastoma cell line.

A. Brothman, D. Fults, B. Williams, 1995, Cancer genetics and cytogenetics.