Localization of MRX82: A new nonsyndromic X-linked mental retardation locus to Xq24-q25 in a Basque family-Reference-Cited by-同舟云学术

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Localization of MRX82: A new nonsyndromic X-linked mental retardation locus to Xq24-q25 in a Basque family

Published:2004-11-03 Issue:2 Volume:131A Page:174-178
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Martínez Francisco,Martínez-Garay Isabel,Oltra Silvestre,Moltó María Dolores,Orellana Carmen,Monfort Sandra,Prieto Félix,Tejada Isabel

Funder

Spanish Ministry of Health (Fondo de Investigación Sanitaria)

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference21 articles.

1. Linkage mapping of a nonspecific form of X-linked mental retardation (MRX53) in a large Pakistani family;Ahmad;Am J Med Genet,2001

2. Linkage analysis suggests at least two loci for X-linked non-specific mental retardation;Arveiler;Am J Med Genet,1988

3. Ultrasensitive staining of nucleic acids with silver;Beidler;Anal Biochem,1982

4. Mapping of a gene for nonspecific X-linked mental retardation (MRX 75) to Xq24-q26;Caspari;Am J Med Genet,2000

5. Characterization of the human glutamate receptor subunit 3 gene (GRIA3): A candidate for bipolar disorder and nonspecific X-linked mental retardation;Gecz;Genomics,1999

Cited by 5 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. Molecular and Clinical Characterization of a Novel Nonsense Variant in Exon 1 of the UPF3B Gene Found in a Large Spanish Basque Family (MRX82);Frontiers in Genetics;2019-10-31

2. Human teneurin-1 is a direct target of the homeobox transcription factor EMX2 at a novel alternate promoter;BMC Developmental Biology;2011-06-08

3. Partial tandem duplication ofGRIA3 in a male with mental retardation;American Journal of Medical Genetics Part A;2007

4. A two base pair deletion in the PQBP1 gene is associated with microphthalmia, microcephaly, and mental retardation;European Journal of Human Genetics;2006-10-11

5. The Basques: Review of Population Genetics and Mendelian Disorders;Human Biology;2005

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