J. Hu

发表

Multipoint imprinting analysis indicates a common precursor cell for gonadal and nongonadal pediatric germ cell tumors.

S. Lauer, Jie Hu, M. Fritsch, 2001, Cancer research.

High-resolution genome-wide allelotype analysis identifies loss of chromosome 14q as a recurrent genetic alteration in astrocytic tumours

H. Ng, J. Hu, J. Pang, 2002, British Journal of Cancer.

Tetrasomy 15q25.3 --> qter resulting from an analphoid supernumerary marker chromosome in a patient with multiple anomalies and bilateral Wilms tumors.

U. Surti, S. Gollin, E. McPherson, 2002, American journal of medical genetics.

Comparative genomic hybridization of esophageal and gastroesophageal adenocarcinomas shows consensus areas of DNA gain and loss

C. Moskaluk, E. Perlman, Jie Hu, 1998, Genes, chromosomes & cancer.

Comparative genomic hybridization analysis of hepatoblastomas

Jie Hu, E. Perlman, B. A. Baker, 2000, Genes, chromosomes & cancer.

Subgroups of uterine leiomyomas based on cytogenetic analysis.

U. Surti, J. Hu, 1991, Human pathology.

Genetic analysis of childhood endodermal sinus tumors by comparative genomic hybridization.

Jie Hu, E. Perlman, R. Castleberry, 2000, Journal of pediatric hematology/oncology.

Cytogenetic analysis of a uterine lipoleiomyoma.

U. Surti, J. Hu, H. Tobon, 1992, Cancer genetics and cytogenetics.

Comparative study of primary and recurrent ovarian serous carcinomas: comparative genomic hybridization analysis with a potential application for prognosis.

U. Surti, M. Jones, J. Hu, 2003, Gynecologic oncology.

Transplantation of congenital primitive neuroectodermal tumor of fetus to the uterus of mother: application of biotin-labeled chromosome-specific probes

U. Surti, P. Dickman, J. Hu, 1994, International Journal of Gynecologic Cancer.

Cryptic duplication of 12q24.33 → qter in a child with Angelman syndrome—simultaneous occurrence of two unrelated cytogenetic events

U. Surti, J. Vockley, J. Bedoyan, 2007, American journal of medical genetics. Part A.