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	1.	Review of the recurrent 8q13.2q13.3 branchio-oto-renal related microdeletion, and report of an additional case with associated distal arthrogryposis. [electronic resource] by Au, Ping-Yee Billie Chernos, Judy E Thomas, Mary Ann Producer: 20171019 In: American journal of medical genetics. Part A vol. 170 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Suitability of rapid aneuploidy detection for prenatal diagnosis. [electronic resource] by Sparkes, Rebecca L Bernier, Francois P Chernos, Judy E Johnson, Jo-Ann M Producer: 20090108 In: Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC vol. 30 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Interstitial deletion of 11q in a mother and fetus: implications of directly transmitted chromosomal imbalances for prenatal genetic counseling. [electronic resource] by Sparkes, Rebecca L Shetty, Shashirekha Chernos, Judy E Mefford, Heather C Micheil Innes, A Producer: 20090423 In: Prenatal diagnosis vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A Challenging Prenatal QF-PCR Rapid Aneuploidy Test Result Caused by a Maternally Inherited Triplication within Chromosome Xq26.2. [electronic resource] by Inkster, Amy Thomas, Mary Ann Gamache, Nadine S Chan, Michael Stenroos, Pernilla Chernos, Judy E Argiropoulos, Bob Publication details: Cytogenetic and genome research 2018 In: Cytogenetic and genome research vol. 156 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Mosaic trisomy 1q: a recurring chromosome anomaly that is a diagnostic challenge and is associated with a Fryns-like phenotype. [electronic resource] by Bone, Kathleen M Chernos, Judy E Perrier, Renee Innes, A Micheil Bernier, Francois P McLeod, Ross Thomas, Mary Ann Producer: 20180509 In: Prenatal diagnosis vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Cytogenetic and molecular characterization of a de-novo cryptic deletion of 7p21 associated with an apparently balanced translocation and complex craniosynostosis. [electronic resource] by Shetty, Shashirekha Boycott, Kym M Gillan, Tanya L Bowser, Kathy Parboosingh, Jillian S McInnes, Brenda Chernos, Judy E Bernier, Francois P Producer: 20071101 In: Clinical dysmorphology vol. 16 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)