A Challenging Prenatal QF-PCR Rapid Aneuploidy Test Result Caused by a Maternally Inherited Triplication within Chromosome Xq26.2 von Inkster, Amy, Thomas, Mary Ann, Gamache, Nadine S., Chan, Michael, Stenroos, Pernilla, Chernos, Judy E., Argiropoulos, Bob

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Review of the recurrent 8q13.2q13.3 branchio-oto-renal related microdeletion, and report of an additional case with associated distal arthrogryposis von Au, Ping-Yee Billie, Chernos, Judy E., Thomas, Mary Ann

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Mosaic trisomy 1q: a recurring chromosome anomaly that is a diagnostic challenge and is associated with a Fryns‐like phenotype von Bone, Kathleen M., Chernos, Judy E., Perrier, Renee, Innes, A. Micheil, Bernier, Francois P., McLeod, Ross, Thomas, Mary Ann

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Suitability of Rapid Aneuploidy Detection for Prenatal Diagnosis von Sparkes, Rebecca L., MD, Bernier, Francois P., MD, Chernos, Judy E., PhD, Johnson, Jo-Ann M., MD

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Interstitial deletion of 11q in a mother and fetus: implications of directly transmitted chromosomal imbalances for prenatal genetic counseling von Sparkes, Rebecca L., Shetty, Shashirekha, Chernos, Judy E., Mefford, Heather C., Micheil Innes, A.

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Mosaic trisomy 1q: a recurring chromosome anomaly that is a diagnostic challenge and is associated with a Fryns-like phenotype: Prenatal diagnosis of mosaic trisomy 1q von Bone, Kathleen M., Chernos, Judy E., Perrier, Renee, Innes, A. Micheil, Bernier, Francois P., McLeod, Ross, Thomas, Mary Ann

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Analysis of sperm chromosome complements from a man heterozygous for a pericentric inversion of chromosome 1 von MARTIN, R. H, CHERNOS, J. E, LOWRY, R. B, PATTINSON, H. A, BARCLAY, L, KO, E

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Effect of cryopreservation on the frequency of chromosomal abnormalities and sex ratio in human sperm von Martin, Renee H., Chernos, Judy E., Rademaker, Alfred W.

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A Challenging Prenatal QF-PCR Rapid Aneuploidy Test Result Caused by a Maternally Inherited Triplication within Chromosome Xq26.2 von Inkster, Amy, Thomas, Mary Ann, Gamache, Nadine S, Chan, Michael, Stenroos, Pernilla, Chernos, Judy E, Argiropoulos, Bob

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Microduplication and Triplication of 22q11.2: A Highly Variable Syndrome von Yobb, Twila M., Somerville, Martin J., Willatt, Lionel, Firth, Helen V., Harrison, Karen, MacKenzie, Jennifer, Gallo, Natasha, Morrow, Bernice E., Shaffer, Lisa G., Babcock, Melanie, Chernos, Judy, Bernier, Francois, Sprysak, Kathy, Christiansen, Jesse, Haase, Shelagh, Elyas, Basil, Lilley, Margaret, Bamforth, Steven, McDermid, Heather E.

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A Comparison of the Frequency of Sperm Chromosome Abnormalities in Men with Mild, Moderate, and Severe Oligozoospermia von MARTIN, Renée H, RADEMAKER, Alfred W, GREENE, Calvin, KO, Evelyn, HOANG, Tina, BARCLAY, Leona, CHERNOS, Judy

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A Novel Method for Generating Xeno-Free Human Feeder Cells for Human Embryonic Stem Cell Culture von Meng, Guoliang, Liu, Shiying, Krawetz, Roman, Chan, Michael, Chernos, Judy, Rancourt, Derrick E.

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Chromosome Abnormalities in Sperm From Infertile Men with Asthenoteratozoospermia von HRISTOVA, Rositsa, KO, Evelyn, GREENE, Calvin, RADEMAKER, Alfred, CHERNOS, Judy, MARTIN, Renée

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Chromosome analysis of spermatozoa extracted from testes of men with non-obstructive azoospermia von Martin, Renée H., Greene, Calvin, Rademaker, Alfred, Barclay, Leona, Ko, Evelyn, Chernos, Judy

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Unusual segregation products in sperm from a pericentric inversion 17 heterozygote von MIKHAAIL-PHILIPS, Monica M, MCGILLIVRAY, Barbara C, HAMILTON, Sara J, KO, Evelyn, CHERNOS, Judy, RADEMAKER, Alfred, MARTIN, Renée H

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Analysis of chromosome segregation in sperm from a chromosome 2 inversion heterozygote and assessment of an interchromosomal effect von Mikhaail-Philips, Monica M., Ko, Evelyn, Chernos, Judy, Greene, Calvin, Rademaker, Alfred, Martin, Renée H.

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Analysis of Aneuploidy in Spermatozoa From Testicular Biopsies From Men With Nonobstructive Azoospermia von Martin, Renée H., Greene, Calvin, Rademaker, Alfred W., Ko, Evelyn, Chernos, Judy

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