Literature DB >> 11186883

Partial trisomy 20p: familial occurrence.

S Oppenheimer1, P Dignan, S Soukup.   

Abstract

Partial trisomy 20p syndrome in an uncle and niece are compared to 32 previous cases.

Entities:  

Mesh：

Year:  2000        PMID： 11186883

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN： 0148-7299


  5 in total

1.  Bayesian Assessment of Genetic Risk in Families with a Balanced Translocation.

Authors:  Douglas VanDerwerken
Journal:  J Genet Couns       Date:  2015-02-04       Impact factor: 2.537

2.  Maternally inherited partial monosomy 9p (pter → p24.1) and partial trisomy 20p (pter → p12.1) characterized by microarray comparative genomic hybridization.

Authors:  Érika L Freitas; Susan M Gribble; Milena Simioni; Társis P Vieira; Roseane L Silva-Grecco; Marly A S Balarin; Elena Prigmore; Ana C Krepischi-Santos; Carla Rosenberg; Karoly Szuhai; Arie van Haeringen; Nigel P Carter; Vera Lúcia Gil-da-Silva-Lopes
Journal:  Am J Med Genet A       Date:  2011-09-21       Impact factor: 2.802

3.  A case of partial trisomy 20p resulting from meiotic recombination of a maternal pericentric inversion.

Authors:  Jeong-Eun Kang; Mi Young Park; Chong Kun Cheon; Hyoung Doo Lee; Sang-Hyun Hwang; Jongyoun Yi
Journal:  Ann Lab Med       Date:  2011-12-20       Impact factor: 3.464

4.  De Novo Pure Trisomy 20p: Report of a Novel Case of a Marker Chromosome and Literature Review.

Authors:  Jungim Choi; Soo Young Yoon; Borae G Park; Baik Lin Eun; Myungshin Kim; Jung Ah Kwon
Journal:  Ann Lab Med       Date:  2020-05       Impact factor: 3.464

5.  Prenatal diagnosis of a de novo trisomy 20p detected by noninvasive prenatal testing.

Authors:  Xu Yan; Haiying Peng; Changjun Zhang
Journal:  Clin Case Rep       Date:  2021-03-11
  5 in total

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