Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles-Reference-Cited by-同舟云学术

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Detection of the fragile X syndrome protein for the evaluation of FMR1 intermediate alleles

Published:2000-08 Issue:2 Volume:107 Page:195-196
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Castellví-Bel Sergi,Fernández-Burriel Miguel,Rifé Maria,Jiménez Dolores,Mallolas Judith,Sánchez Aurora,Ramos Feliciano,Milà Montserrat

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s004390000349.pdf

Cited by 6 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. Autistic Phenotype of Permutation and Intermediate Alleles of FMR1 Gene;Iranian Journal of Pediatrics;2017-07-26

2. Guía clínica de las enfermedades asociadas al gen FMR1: síndrome X frágil, insuficiencia ovárica primaria y síndrome de temblor-ataxia;Medicina Clínica;2014-03

3. Fragile-X syndrome and fragile X-associated tremor/ataxia syndrome: two faces of FMR1;The Lancet Neurology;2007-01

4. An Investigation of FRAXA Intermediate Allele Phenotype in A Longitudinal Sample;Annals of Human Genetics;2006-03

5. FMR1 alleles in Tasmania: a screening study of the special educational needs population;Clinical Genetics;2004-10-20

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