Literature DB >> 21039433

CCMG guidelines: prenatal and postnatal diagnostic testing for uniparental disomy.

A J Dawson1, J Chernos, J McGowan-Jordan, J Lavoie, S Shetty, M Steinraths, J-C Wang, J Xu.   

Abstract

The aim of this statement is to provide clinicians, cytogeneticists and molecular geneticists of the Canadian College of Medical Geneticists (CCMG) a comprehensive review of the role of UPD in constitutional genetic diagnosis and to provide a guideline as to when investigation for UPD is recommended. Members of the CCMG Cytogenetics, Molecular Genetics, Clinical Practice, and Prenatal Diagnosis committees reviewed the relevant literature on uniparental disomy (UPD) in constitutional genetic diagnosis (May 2010). Guidelines were developed for UPD testing in Canada. The guidelines were circulated for comment to the CCMG members at large and following appropriate modification, approved by the CCMG Board of Directors (July 2010).
© 2010 John Wiley & Sons A/S.

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Mesh:

Year:  2010        PMID: 21039433     DOI: 10.1111/j.1399-0004.2010.01547.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  13 in total

Review 1.  The mechanisms and clinical application of mosaicism in preimplantation embryos.

Authors:  Xinyuan Li; Yan Hao; Nagwa Elshewy; Xiaoqian Zhu; Zhiguo Zhang; Ping Zhou
Journal:  J Assist Reprod Genet       Date:  2019-12-14       Impact factor: 3.412

Review 2.  Genetic basis of single-suture synostoses: genes, chromosomes and clinical implications.

Authors:  Wanda Lattanzi; Nenad Bukvic; Marta Barba; Gianpiero Tamburrini; Camilla Bernardini; Fabrizio Michetti; Concezio Di Rocco
Journal:  Childs Nerv Syst       Date:  2012-08-08       Impact factor: 1.475

Review 3.  Uniparental disomy in Robertsonian translocations: strategies for uniparental disomy testing.

Authors:  Moh-Ying Yip
Journal:  Transl Pediatr       Date:  2014-04

4.  Paternal uniparental disomy for chromosome 14: prenatal management.

Authors:  Joana Isabel Igreja da Silva; Barbara Ribeiro; Alexandra Cadilhe; Cristina Nogueira-Silva
Journal:  BMJ Case Rep       Date:  2019-12-30

5.  Phenotypic spectrum in uniparental disomy: Low incidence or lack of study?

Authors:  Arpan D Bhatt; Thomas Liehr; Sonal R Bakshi
Journal:  Indian J Hum Genet       Date:  2013-07

6.  Mosaic partial pericentromeric trisomy 8 and maternal uniparental disomy in a male patient with autism spectrum disorder.

Authors:  Dina F Ahram; Danae Stambouli; Aleksandra Syrogianni; Yasser Al-Sarraj; Spyridon Gerou; Hatem El-Shanti; Marios Kambouris
Journal:  Clin Case Rep       Date:  2016-10-21

7.  Uniparental disomy and prenatal phenotype: Two case reports and review.

Authors:  Xiaofei Li; Yan Liu; Song Yue; Li Wang; Tiejuan Zhang; Cuixia Guo; Wenjie Hu; Karl-Oliver Kagan; Qingqing Wu
Journal:  Medicine (Baltimore)       Date:  2017-11       Impact factor: 1.817

Review 8.  Chromosomal Mosaicism in Human Feto-Placental Development: Implications for Prenatal Diagnosis.

Authors:  Francesca Romana Grati
Journal:  J Clin Med       Date:  2014-07-24       Impact factor: 4.241

9.  Prenatal diagnosis of complete maternal uniparental isodisomy of chromosome 4 in a fetus without congenital abnormality or inherited disease-associated variations.

Authors:  WeiQiang Liu; HuiMin Zhang; Jian Wang; GuoJiu Yu; WenJun Qiu; ZhiHua Li; Min Chen; Kwong Wai Choy; XiaoFang Sun
Journal:  Mol Cytogenet       Date:  2015-11-04       Impact factor: 2.009

10.  Uniparental disomy as a cause of pediatric endocrine disorders.

Authors:  Keiko Matsubara; Masayo Kagami; Maki Fukami
Journal:  Clin Pediatr Endocrinol       Date:  2018-07-31
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