Citations (16)
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E. N. Kontomanolis, P. Pandya & V. Limperis. (2010) Trisomy 22: The heart aspect. Journal of Obstetrics and Gynaecology 30:6, pages 627-628.
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Yun Yan Qu, Li Yu Xing, Elizabeth D. Hughes & Thomas L. Saunders. (2008) Chromosome Dropper Tool: Effect of Slide Angles on Chromosome Spread Quality for Murine Embryonic Stem Cells. Journal of Histotechnology 31:2, pages 75-79.
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Articles from other publishers (14)
Valentina Trevisan, Anna Meroni, Chiara Leoni, Fabio Sirchia, Davide Politano, Giacomo Fiandrino, Valentina Giorgio, Donato Rigante, Domenico Limongelli, Lucrezia Perri, Elisabetta Sforza, Francesca Leonardi, Germana Viscogliosi, Ilaria Contaldo, Daniela Orteschi, Luca Proietti, Giuseppe Zampino & Roberta Onesimo. (2024) Trisomy 22 Mosaicism from Prenatal to Postnatal Findings: A Case Series and Systematic Review of the Literature. Genes 15:3, pages 346.
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Aline Nardelli, Larissa Valéria Laskoski, Andressa Fernanda Luiz, Maruhen Amir Datsch Silveira & Luciana Paula Grégio d’Arce. (2023) Occurrence of mosaic trisomy 22 and pericentric inversion of chromosome 9 in a patient with a good prognosis. BMC Medical Genomics 16:1.
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Arundhati Gosavi, Nora Izzati Hj Ali Mashod, Jocelyn Ziqi Quek, Sarah Aung, Stephie Siew Fong Chin, Biswas Arijit & Sherry Sze Yee Ho. (2023) Case studies of fetal mosaicisms detected by non-invasive prenatal testing. Annals of the Academy of Medicine, Singapore 52:1, pages 41-43.
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Athanasia Warnecke & Anja Giesemann. (2021) Embryologie, Fehlbildungen und seltene Erkrankungen der
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Virginia Miraldi Utz, Diana S. Brightman, Monica A. Sandoval, Robert B. Hufnagel & Howard M. Saal. (2020)
Systemic and ocular manifestations of a patient with mosaic
ARID1A
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Samira Kalayinia, Tina Shahani, Alireza Biglari, Majid Maleki, Hassan Rokni‐Zadeh, Zahra Razavi & Nejat Mahdieh. (2018) Mosaic trisomy 22 in a 4‐year‐old boy with congenital heart disease and general hypotrophy: A case report. Journal of Clinical Laboratory Analysis 33:2.
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Mario Zanolli, Alex V. Levin & Guillermo Lay-Son. 2017. The Eye in Pediatric Systemic Disease. The Eye in Pediatric Systemic Disease
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Fabiola Quintero‐Rivera & Julian A. Martinez‐Agosto. (2013) Hemifacial microsomia in cat‐eye syndrome: 22q11.1–q11.21 as candidate loci for facial symmetry. American Journal of Medical Genetics Part A 161:8, pages 1985-1991.
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Dalal Abdelgadir, Malgorzata J.M. Nowaczyk & Chumei Li. (2013) Trisomy 22 Mosaicism and Normal Developmental Outcome: Report of Two Patients and Review of the Literature. American Journal of Medical Genetics Part A 161:5, pages 1126-1131.
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M.C. Herwig, A.M. Müller, F.G. Holz & K.U. Loeffler. (2010) Analyse eines ophthalmopathologischen Kollektivs humaner fetaler Augen unter besonderer Berücksichtigung außergewöhnlicher BefundeAnalysis of an ophthalmic pathology cohort of human fetal eyes with regard to interesting findings. Der Ophthalmologe 107:11, pages 1051-1058.
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Sandrine Leclercq, Xavier Baron, Marie‐Line Jacquemont, Fabrice Cuillier & François Cartault. (2009) Mosaic trisomy 22: five new cases with variable outcomes. Implications for genetic counselling and clinical management. Prenatal Diagnosis 30:2, pages 168-172.
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Gordana Raca, Lisa Schimmenti & Christa Lese Martin. (2008) Intrachromosomal duplications of 22q11 are not a common cause of isolated coloboma and coloboma with other limited features of cat eye syndrome. American Journal of Medical Genetics Part A 146A:3, pages 401-404.
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Jia‐Chi Wang, Linda Dang, Tapas Kumar Mondal & Aneal Khan. (2007) Prenatally diagnosed mosaic trisomy 22 in a fetus with left ventricular non‐compaction cardiomyopathy. American Journal of Medical Genetics Part A 143A:22, pages 2744-2746.
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Meghan Delaney & Theonia K. Boyd. (2008) Case Report of Unilateral Clefting: Is Sonic Hedgehog to Blame?. Pediatric and Developmental Pathology 10:2, pages 117-120.
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