Bixia Xiang

发表

Three-color cDNA microarrays with prehybridization quality control yield gene expression data comparable to that of commercial platforms.

M. Hessner, Xujing Wang, Lisa Meyer, 2006, Physiological genomics.

Navigating Web-Based Resources for Genetic Testing of Chromosome Abnormalities, CNVs and Gene Mutations

Bixia Xiang, Deqiong Ma, 2014 .

Pulmonary atresia with intact ventricular septum (PA‐IVS) in monozygotic twins

P. Hui, Peining Li, E. Zambrano, 2008, American journal of medical genetics. Part A.

Maternal uniparental disomy of chromosome 15 and concomitant STRC and CATSPER2 deletion‐mediated deafness‐infertility syndrome

Wahab A. Khan, S. Scott, Amy C Yang, 2017, American journal of medical genetics. Part A.

Genomic characterization of prenatally detected chromosomal structural abnormalities using oligonucleotide array comparative genomic hybridization

Fang Xu, M. Mahoney, Peining Li, 2011, American journal of medical genetics. Part A.

Double-minute MYC amplification and deletion of MTAP, CDKN2A, CDKN2B, and ELAVL2 in an acute myeloid leukemia characterized by oligonucleotide-array comparative genomic hybridization.

R. Bajaj, Peining Li, Bixia Xiang, 2008, Cancer genetics and cytogenetics.

Short communication Double-minute MYC amplification and deletion of MTAP, CDKN2A, CDKN2B, and ELAVL2 in an acute myeloid leukemia characterized by oligonucleotide-array comparative genomic hybridization

R. Bajaj, Peining Li, Bixia Xiang, 2008 .

Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disability

Hongyu Zhao, V. Schulz, P. Gallagher, 2014, Molecular Cytogenetics.

Analytical and clinical validity of whole‐genome oligonucleotide array comparative genomic hybridization for pediatric patients with mental retardation and developmental delay

Hongyu Zhao, N. Nowak, Peining Li, 2008, American journal of medical genetics. Part A.

Evidence-based genomic diagnosis characterized chromosomal and cryptic imbalances in 30 elderly patients with myelodysplastic syndrome and acute myeloid leukemia

Bixia Xiang, Peining Li, Stephanie Halene, 2011, Molecular Cytogenetics.

Clinical and genomic characterization of distal duplications and deletions of chromosome 4q: Study of two cases and review of the literature

M. Seashore, H. Kaymakçalan, M. Mahoney, 2009, American journal of medical genetics. Part A.

Comprehensive quality control utilizing the prehybridization third-dye image leads to accurate gene expression measurements by cDNA microarrays

Nan Jiang, Shuang Jia, Howard J. Jacob, 2006, BMC Bioinformatics.

Genome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation: a multicenter experience of 1499 clinical cases.

Marilyn M. Li, Yiping Shen, David T. Miller, 2010, The Journal of molecular diagnostics : JMD.

Noninvasive prenatal testing of α-thalassemia and β-thalassemia through population-based parental haplotyping

Peixiang Ni, Zhiyu Peng, Jian Li, 2021, Genome medicine.

Cytogenomic mapping and bioinformatic mining reveal interacting brain expressed genes for intellectual disability

V. Schulz, P. Gallagher, Fang Xu, 2014, Molecular Cytogenetics.

Genome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation: a multicenter experience of 1499 clinical cases.

Marilyn M. Li, Yiping Shen, David T. Miller, 2010, The Journal of molecular diagnostics : JMD.

Genomic characterization of prenatally detected chromosomal structural abnormalities using oligonucleotide array comparative genomic hybridization

Fang Xu, M. Mahoney, Peining Li, 2011, American journal of medical genetics. Part A.