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Carrier testing for Mendelian and cytogenetic disorders in potential sperm donors; The importance of genetic counseling

J. Basile, and A. Donnenfeld

Carrier Testing for Seven Diseases Common in eastern European (Ashkenazi) Jewish Population: Implications for Counseling and Testing

Elaine A. Sugarman, M.S., C.G.C. and Bernice A. Allitto, Ph.D.

Case Study: Four color flow cytometry identifies B-cell chronic lymphocytic leukemia case with two distinct clones of ZAP-70 postive and negative neoplastic b-lymphoid cells

S.J. Fabello, K. Baggiani, L. Hertzberg, T. Oldaker
Genzyme Genetics/Impath, Los Angeles, CA

Case Study: Four color flow cytometry identifies mast cell presence in bone marrow specimen submitted for suspected systemic mastocytosis

Roderick Redor, Christopher Felten, Karina Baggiani, Syndette Fabello, Lawrence Hertzberg, Teri Oldaker
Genzyme Genetics/Impath, Los Angeles, CA

Causes of discrepancy between prenatal chromosome results and phenotypic sex

Kempf T., Donnenfeld A.E., Puck S.

CFTR Mutation Distribution among U.S.-Hispanic & African American Individuals: Evaluation in Known Affected and Carrier Screening Populations

E.A. Sugarman, E.M. Rohlfs, B.A. Allitto

Characterization of a Variant of Unknown Significance for Finnish Congenital Nephrosis in the NPHS1 gene

M. McCoy1, R. Sinow2, N. Nagan3, H. Zhu3, S. Bhatt1
1Genzyme Genetics, CA, 2Magella Medical Group, Torrance, CA, 3Genzyme Genetics, Westborough, MA

Characterization of Prenatally Diagnosed Marker Chromosomes; an analysis of 185 cases from 491,596 amniocentesis samples

F. Wallace, A. Donnenfeld, S. Berend, M. Shaham

Chromatin features imply segregation of parental genomes and epigenetic involvement

Jyoti P. Chaudhuri, Sultan Karamanov, Mathew Battaglia, Joachim-U. Walther
Tumour Cytogenetic Unit, Kinderklinik, LMU, 80336 Munich, FRG 2 Genedia GmbH, 80337 Munich, FRG 3 Genzyme Genetics, Phoenix, AZ 85034, USA.

Chromosome abnormalities among fetuses with pleural effusions detected on prenatal ultrasound examination: Comparison of aneuploidy rates between isolated pleural effusions and those with other congenital anomalies.

K Waller, MS, T Custer, AE Donnelfeld

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