Pubdiz
Taipei Medical University

Pubdiz from Gene to Disease ��] ��Ʈw

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Gene Symbol
Gene NameAliasesPrevious_Symbol

FRAXF

fragile site, folic acid type, rare, fra(X)(q28)


Gene FRAXF gene interaction
View Neighborhood Gene

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MeSH term
FrequencyCondition_Probility

Alleles

30.0

Amino Acid Sequence

30.0

Humans

160.0

Molecular Sequence Data

80.0

Research Support, Non-U.S. Gov't

130.0

Female

130.0

Infant, Newborn

30.0

Male

120.0

Mental Retardation/genetics

21.0

Polymerase Chain Reaction/*methods

20.0

Sex Factors

20.0

Chromosome Fragile Sites

75.0

*Chromosome Fragility

75.0

Cloning, Molecular

40.0

*Trinucleotide Repeats

43.0

*X Chromosome

50.0

Base Sequence

80.0

Blotting, Southern

20.0

Gene Frequency

20.0

Pedigree

50.0

Research Support, U.S. Gov't, P.H.S.

30.0

Adult

30.0

Child, Preschool

20.0

Microsatellite Repeats

20.0

DNA Primers

30.0

Polymerase Chain Reaction

40.0

Genetic Markers

40.0

Child

20.0

Fragile X Syndrome/*genetics

63.0

In Situ Hybridization, Fluorescence

20.0

Brain/metabolism

20.0

Dinucleoside Phosphates

211.0

Mental Retardation/*genetics

20.0

*Nuclear Proteins

20.0

Proteins/*genetics

20.0

*Repetitive Sequences, Nucleic Acid

30.0

Research Support, U.S. Gov't, Non-P.H.S.

20.0

Sequence Homology, Amino Acid

20.0

*Trans-Activators

20.0

Transcription, Genetic

20.0

Methylation

20.0

X Chromosome/*ultrastructure

28.0