Skip to search formSkip to main contentSkip to account menu

AFF2 gene

Known as: AF4/FMR2 family member 2, FRAXE, AF4/FMR2 FAMILY, MEMBER 2 
National Institutes of Health

Related topics

Related topics

1 relation
FRAXE Syndrome

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Extensão rural agroecológica: uma estratégia para a multiplicação de conhecimentos agroecológicos em comunidades ribeirinhas no amazonas
Jozane Lima Santiago, Albejamere Pereira de Castro, Therezinha de Jesus Pinto Fraxe, Marília Gabriela Gondim Rezende e Janaína de… 
2012
2012
FRAXE molecular diagnosis in individuals referred for FRAXA screening
FRAXE mental retardation is a form of mild to moderate intellectual disability generally associated with learning difficulties… 
2011
2011
Evaluating the influence of four variants detected in the FRAXA and FRAXE loci
2010
2010
FMR2 gene deletion as a cause of non-specific mental retardation and autistic behavior in two brothers
2006
2006
Original Communication Fragile X screening for FRAXA and FRAXE mutations using PCR based studies: Results of a five year study
28 . The frequency of occurrence of Fragile X syndrome is estimated to be 1/4000 male births. Screening of refer­ rals for the… 
2000
2000
FRAXE mutation in a mentally retarded subject and in his phenotypically normal twin brother
The FRAXE fragile site, 600 kb distal to the more common FRAXA, has been reported to be expressed in subjects with mild non… 
1999
1999
Microdeletions in FMR 2 may be a significant cause of premature ovarian failure
Genetic causes of premature ovarian failure (POF) include X chromosome deletions and fragile X (FRAXA) premutations. While… 
1998
1998
FRAXE : the HindIII/OXE20 restriction polymorphism is not a rare variant
FRAXE, a fragile site located in Xq28, is associated with a mild mental impairment. It results from a (CCG) trinucleotide… 
1997
1997
DNA study of FRAXA and FRAXE in Chinese children with neurodevelopmental disorders