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A Rare Case of ins(1)(p22.3q25q32.1) Reported In a Patient With Unbalanced Offspring

Rosemarie Schmidt, MS, CLSp(CG), Stefania Rondinelli, BA, ClSp(CG), Eva Beller, MS,Veena Suri, PhD, Martha Weinstein, PhD,

A rare case of possible 3;1 meiotic segregation and subsequent interchange trisomy 18 in a fetus whose mother carries a t(12;18) (p13.1;q21.1) translocation

Christin M. Coffeen1, Sucheta Bhatt1, Maya Thangavelu1, David B. Rogers1, Lawrence D. Platt2, 3
1Genzyme Genetics, Orange, CA; 2David Geffen School of Medicine at UCLA, Los Angeles, CA; 3Center for Fetal Medicine and Women's Ultrasound, Los Angeles

A retrospective study of 27,123 products of conception submitted for cytogenetic analysis

Judith Knops, Ph.D., Jacque Hansen, Alicia Navoy, Alan Donnenfeld, M.D.

A simple agarose gel-based PCR for detection and sizing of trinucleotide repeats in fragile X syndrome

A. Hajianpour, S. LIang, W. Bai, S. Kou, R. Habibian, J.C. Wang.
Genzyme Genetics, Pasadena, CA

Acute myeloid leukemia with high side scatter and lack of blastic markers; flow cytometric parameters that help to differentiate from benign conditions and acute promyelocytic leukemia

W. Gorczyca, J. Weisberger, C.D. Wu, H.Y. Dong, and Z. Liu
Genzyme Genetics Hematopathology Laboratory, New York, NY, and Bio-Reference Laboratory, Elmwood, NJ

Amniotic Fluid Cytogenetic Analysis Turn-Around Time-Comparison of Aneuploid And Diploid Samples

Alan E. Donnenfeld, MD, David Lockwood, PhD, Fei Wang, MS, Trace Custer, BA