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Judy Chernos

Alberta Children's Hospital

17

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390

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Clinical and molecular characterization of an almost complete ring chromosome 4 in two sisters, with recurrence due to gonadal mosaicism.

2021 Clinical Dysmorphology
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Prenatal Array Comparative Genomic Hybridization in Fetuses With Structural Cardiac Anomalies.

2016 Journal of obstetrics and gynaecology Canada
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MG-130 Pure duplication of 1q42.11-q44(QTER): Further clinical delineation of a rare terminal duplication syndrome

2015 Journal of Medical Genetics
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MG-140 17Q21.31 microdeletion syndrome: A description of two cases

2015 Journal of Medical Genetics
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A 2q24.3q31.1 microdeletion found in a patient with Filippi-like syndrome phenotype: a case report.

2014 American Journal of Medical Genetics Part A
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Canadian College of Medical Geneticists guidelines for the indications, analysis, and reporting of cancer specimens.

2011 Current Oncology
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CCMG Guidelines for Genomic Microarray Testing

2010
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Cri du chat syndrome due to meiotic recombination in a pericentric inversion 5 carrier

2008 Clinical Genetics
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Shedding new light on false positive diagnosis of trisomy 21 by fluorescence in situ hybridization (FISH) on uncultured amniotic fluid cells: experiences from two Canadian cytogenetic laboratories

2007 Prenatal Diagnosis
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Chromosome analysis of spermatozoa extracted from testes of men with non-obstructive azoospermia

2000 Genetics in Medicine
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