Concurrence of fragile X and Klinefelter syndromes: report of a new case of paternal nondisjunction-Reference-Cited by-同舟云学术

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Concurrence of fragile X and Klinefelter syndromes: report of a new case of paternal nondisjunction

Published:2003-01 Issue:1 Volume:46 Page:53-55
ISSN:0003-3995
Container-title:Annales de Génétique
language:en
Short-container-title:Annales de Génétique

Author:

Santos Cíntia Barros,Hjalgrim Helle,Carneiro Flávia Raquel Gonçalves,Ribeiro Márcia,Boy Raquel Tavares,Pimentel Márcia Mattos Gonçalves

Publisher

Elsevier BV

Subject

Genetics

Reference21 articles.

1. Human and murine FMR1: evidence for alternative splicing and translational initiation downstream of the CGG-repeat;Ashley;Nat. Genet.,1993

2. Prevalence and phenotype consequence of FRAXA and FRAXE alleles in a large, ethnically diverse, special education-needs population;Crawford;Am. J. Hum. Genet.,1999

3. Fragile X mutation and Klinefelter syndrome: a reappraisal;Filippi;Am. J. Med. Genet.,1988

4. Screening for fra(X)(q) in a population of mentally retarded males;Froster-Iskenius;Hum. Genet.,1983

5. XY/XXY mosaicism and fragile X syndrome;Fryns;Ann. Genet.,1983

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Fragile sites, chromosomal lesions, tandem repeats, and disease;Frontiers in Genetics;2022-11-17

2. Folate deficiency drives mitotic missegregation of the human FRAXA locus;Proceedings of the National Academy of Sciences;2018-12-03

3. Male-to-male transmission of X-linked Alport syndrome in a boy with a 47,XXY karyotype;European Journal of Human Genetics;2005-06-15

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