First prenatal case of Kagami-Ogata syndrome associated with a small supernumerary marker chromosome derived from chromosome 15-Reference-Cited by-同舟云学术

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First prenatal case of Kagami-Ogata syndrome associated with a small supernumerary marker chromosome derived from chromosome 15

Published:2022-03 Issue:2 Volume:61 Page:382-384
ISSN:1028-4559
Container-title:Taiwanese Journal of Obstetrics and Gynecology
language:en
Short-container-title:Taiwanese Journal of Obstetrics and Gynecology

Author:

Receveur Aline,Puisney-Dakhli Chloé,Kleinfinger Pascale,Gitz Laurence,Grevoul-Fesquet Julie,Jouni Dima,Diot Romain,Tachdjian Gérard,Petit François

Publisher

Elsevier BV

Subject

Obstetrics and Gynecology

Reference15 articles.

1. Paternal uniparental isodisomy for chromosome 14 in a patient with a normal 46,XY karyotype;Chu;Am J Med Genet,2004

2. Human imprinting disorders: principles, practice, problems and progress;Mackay;Eur J Med Genet,2017

3. A male case of Kagami-Ogata syndrome caused by paternal unipaternal disomy 14 as a result of a Robertsonian translocation;Wang;Front Pediatr,2020

4. Deletions and epimutations affecting the human 14q32.2 imprinted region in individuals with paternal and maternal upd(14)-like phenotypes;Kagami;Nat Genet,2008

5. De novo small supernumerary marker chromosomes arising from partial trisomy rescue;Matsubara;Front Genet,2020

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