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	21.	Establishment and characterization of fetal and maternal mesenchymal stem/stromal cell lines from the human term placenta. [electronic resource] by Qin, Sharon Q Kusuma, Gina D Al-Sowayan, Batla Pace, Rishika A Isenmann, Sandra Pertile, Mark D Gronthos, Stan Abumaree, Mohamed H Brennecke, Shaun P Kalionis, Bill Producer: 20170103 In: Placenta vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	A fetus coexisting with a complete hydatidiform mole with trisomy 9 of maternal origin. [electronic resource] by Kan, Anita Sik Yau Lau, Elizabeth Tak Kwong So, Chun Hong Chan, Wan Pang Wong, Wing Cheuk Lee, Kam Cheong Pertile, Mark D Tang, Mary Hoi Yin Producer: 20181022 In: The journal of obstetrics and gynaecology research vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	High-throughput analysis of chromosome abnormality in spontaneous miscarriage using an MLPA subtelomere assay with an ancillary FISH test for polyploidy. [electronic resource] by Bruno, Damien L Burgess, Trent Ren, Hua Nouri, Sara Pertile, Mark D Francis, David I Norris, Fiona Kenney, Bronwyn K Schouten, Jan Andy Choo, K H Slater, Howard R Producer: 20070125 In: American journal of medical genetics. Part A vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	Exceptional complex chromosomal rearrangements in three generations. [electronic resource] by Kartapradja, Hannie Marzuki, Nanis Sacharina Pertile, Mark D Francis, David Suciati, Lita Putri Anggaratri, Helena Woro Ambarwati, Debby Dwi Idris, Firman Prathama Lesmana, Harry Trimarsanto, Hidayat Paramayuda, Chrysantine Harahap, Alida Roswita Producer: 20150227 In: Case reports in genetics vol. 2015 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	Isochromosome 21q is overrepresented among false-negative cell-free DNA prenatal screening results involving Down syndrome. [electronic resource] by Huijsdens-van Amsterdam, Karin Page-Christiaens, Lieve Flowers, Nicola Bonifacio, Michael D Ellis, Katie M Battese Vogel, Ida Vestergaard, Else Marie Miguelez, Javier de Carvalho, Mario Henrique Burlacchini Sistermans, Erik A Pertile, Mark D Producer: 20190308 In: European journal of human genetics : EJHG vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Haplotyping the human leukocyte antigen system from single chromosomes. [electronic resource] by Murphy, Nicholas M Burton, Matthew Powell, David R Rossello, Fernando J Cooper, Don Chopra, Abha Hsieh, Ming Je Sayer, David C Gordon, Lavinia Pertile, Mark D Tait, Brian D Irving, Helen R Pouton, Colin W Producer: 20180423 In: Scientific reports vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Offering pregnant women different levels of genetic information from prenatal chromosome microarray: a prospective study. [electronic resource] by Halliday, Jane L Muller, Cecile Charles, Taryn Norris, Fiona Kennedy, Joanne Lewis, Sharon Meiser, Bettina Donath, Susan Stark, Zornitza McGillivray, George Menezes, Melody Smith, Sian K Forster, Della Walker, Susan Pertile, Mark Amor, David J Producer: 20181226 In: European journal of human genetics : EJHG vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Unstable Robertsonian translocations der(13;15)(q10;q10): heritable chromosome fission without phenotypic effect in two kindreds. [electronic resource] by Perry, Jo White, Sue M Nouri, Sara Bain, Sharon M Hutchinson, Rhonda G La, Phung Northrop, Emma Eyre, Helen J Pertile, Mark D Hocking, Trudy A Thompson, Elizabeth M Yu, Sui Choo, K H Andy Slater, Howard R Producer: 20050810 In: American journal of medical genetics. Part A vol. 136 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	A minimum estimate of the prevalence of 22q11 deletion syndrome and other chromosome abnormalities in a combined prenatal and postnatal cohort. [electronic resource] by Hui, Lisa Poulton, Alice Kluckow, Eliza Lindquist, Anthea Hutchinson, Briohny Pertile, Mark D Bonacquisto, Leonard Gugasyan, Lucy Kulkarni, Abhijit Harraway, James Howden, Amanda McCoy, Richard Costa, Fabricio Da Silva Menezes, Melody Palma-Dias, Ricardo Nisbet, Debbie Martin, Nicole Bethune, Michael Poulakis, Zeffie Halliday, Jane Producer: 20210427 In: Human reproduction (Oxford, England) vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	Association between timing of diagnosis of trisomy 21, 18, and 13 and maternal socio-economic status in Victoria, Australia: A population-based cohort study from 2015 to 2016. [electronic resource] by Kluckow, Eliza Halliday, Jane Poulton, Alice Lindquist, Anthea Hutchinson, Briohny Bethune, Michael Bonacquisto, Leonard Da Silva Costa, Fabricio Gugasyan, Lucy Harraway, James Howden, Amanda Kulkarni, Abhijit Martin, Nicole McCoy, Richard Menezes, Melody Nisbet, Debbie Palma-Dias, Ricardo Pertile, Mark D Poulakis, Zeffie Hui, Lisa Producer: 20200810 In: Prenatal diagnosis vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Correction: Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 tests. [electronic resource] by Archibald, Alison Dalton Smith, Melanie Jane Burgess, Trent Scarff, Katrina Louise Elliott, Justine Hunt, Clare Elizabeth Barns-Jenkins, Caitlin Holt, Chelsea Sandoval, Karina Kumar, Vanessa Siva Ward, Lisa Allen, Emily Caroline Collis, Sarah Valerie Cowie, Shannon Francis, David Delatycki, Martin B Yiu, Eppie Mildred Massie, R John Pertile, Mark Domenic du Sart, Desirée Bruno, Damien Amor, David J Publication details: Genetics in medicine : official journal of the American College of Medical Genetics 11 2018 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Reproductive genetic carrier screening for cystic fibrosis, fragile X syndrome, and spinal muscular atrophy in Australia: outcomes of 12,000 tests. [electronic resource] by Archibald, Alison Dalton Smith, Melanie Jane Burgess, Trent Scarff, Katrina Louise Elliott, Justine Hunt, Clare Elizabeth McDonald, Zoe Barns-Jenkins, Caitlin Holt, Chelsea Sandoval, Karina Siva Kumar, Vanessa Ward, Lisa Allen, Emily Caroline Collis, Sarah Valerie Cowie, Shannon Francis, David Delatycki, Martin B Yiu, Eppie Mildred Massie, R John Pertile, Mark Domenic du Sart, Desirée Bruno, Damien Amor, David J Producer: 20180926 In: Genetics in medicine : official journal of the American College of Medical Genetics vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)