M. Jamehdor

HER-2/neu Testing in Breast Carcinoma: A Combined Immunohistochemical and Fluorescence In Situ Hybridization Approach

R. Ridolfi, M. Jamehdor, J. M. Arber, 2000, Modern Pathology.

Genetic Services in the KP Southern California Region: Delivering the Promises of Tomorrow Today.

M. Jamehdor, M. Alvarado, N. Shinno, 2006, The Permanente journal.

Miller-Dieker Syndrome: Detection of a Cryptic Chromosome Translocation Using In Situ Hybridization in a Family With Multiple Affected Offspring

P. Jacob, H. Bass, M. Jamehdor, 1993 .

Incomplete EEC syndrome in a patient with mosaic monosomy 21.

S. Pruzansky, C. Kaye, M. Jamehdor, 1978, The Cleft palate journal.

Donor origin of a posttransplant liver allograft malignancy identified by fluorescence in situ hybridization for the Y chromosome and DNA genotyping.

W. Grody, R. Busuttil, J. Donovan, 1997, Transplantation.

Identification of an unusual marker chromosome by spectral karyotyping.

Y. Ning, T. Ried, A. Lamb, 1998, American journal of medical genetics.

A pseudo-full mutation identified in fragile X assay reveals a novel base change abolishing an EcoRI restriction site.

Hanlin Gao, C. Astbury, H. Bass, 2008, Journal of Molecular Diagnostics.