Posters

A Case of 45, X 46, X, r(X) Detected Prenatally

C. McKenna, L.S. Heckman, R. Schmidt, M. Moretti, A. Yenamandra, P. Koduru, L. Mehta
Genzyme Genetics, St. Vincents Medical Center, Staten Island, NY, North Shore University Hospital, Manhasset, NY

A Case of 46, XY, r(5)(p15.3q35) 45, XY,-5 Detected In A Child With Mental Retardation

Karina Shapiro, MS, Rosemarie Schmidt, MS, Veena Suri, PhD, Martha Weinstein, PhD

A case of DER(7)INS(7;8)(Q21.2; Q24.1Q22) detected in an infant with facial asymmetry and cleft palate

Rosemarie Schmidt, M.S.¹, Agnieszka Gorski, B.S.¹, Veena Suri, Ph.D.¹, J. Britt Ravnan. Ph.D.², Eve Beller,M.S.³, Martha Weinstein, Ph.D.¹
¹Genzyme Genetics, Yonkers, NY, ²Genzyme Genetics, Santa Fe, NM, ³Kings County Hospital, NY

A case of trisomy 8 and DIC(9;12)(P13;P13) detected in the bone marrow of a child

Rosemarie Schmidt, M.S., Veena Suri, Ph.D., Gabrielle Jervis, M.S., Martha Weinstein, Ph.D.
Genzyme Genetics, Yonkers, NY, Genzyme Genetics, Tampa, FL

A FIVE BREAK FAMILIAL COMPLEX REARRANGEMENT

Pedro Nuno dos Santo, BS.¹, Marjorie McGivans, BS.¹, Rosemarie Schmidt, MS.¹, Veena Suri, Ph.D.¹, Meira Shaham, Ph.D¹, J. Britt Ravnan, Ph.D.²
¹Genzyme Genetics, Yonkers, NY, ²Genzyme Genetics, Santa Fe, NM.

A five-way translocation in acute promyelocytic leukemia

K. Koniecko, CLSp(CG), S.Y. Dong, M.D., CLSp(CG), S. Karamanov, M.D., CLSp(CG), CLSp(MB), C Berger, CLSup, DC Stegeman, M.S., M.B.A., CL Dir., C.F. Stephenson, Ph.D., FACMG
IMPATH, Phoenix, AZ

A novel four-color direct staining multi-site validation of Zap 70 using a variety of specimen types and patient diagnosis in a clinical laboratory setting

K. Baggiani, X. Li, S. Fabello, L. Hertzberg, S. Tugulea, T. Oldaker
Genzyme Genetics/Impath, Losangeles, CA

A novel jumping translocation in a case of acute myeloid leukemia

J Tsai, M. Thangavelu, W. Tom, B. Huang
Genzyme Genetics, Orange, CA

A One-on-one Method for Assessing and Improving Bilingual abilities for a Genetic Counselor learning Spanish

Tammy Ader, Tammy Levy, Deborah Durand
Genzyme Genetics, Miami, Florida

A Polymorphism at the Diagnostic SNRPN Not I site Produces Atypical Methylation Patterns in Analysis for Prader-Willi Syndrome

Jean M. DeMarchi, Ph.D., Scott Chartrand, B.S., Michelle Thackston, B.S., Karen Treat, M.S., C.G.C., and Bernice A. Allitto, Ph.D.