|
| Entrez Id: |
4204 |
| Gene Symbol: |
MECP2 |
MECP2
|
0.400 |
CausalMutation
|
phenotype |
CLINVAR |
Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome.
|
15057977 |
2004 |
|
| Entrez Id: |
4204 |
| Gene Symbol: |
MECP2 |
MECP2
|
0.400 |
GeneticVariation
|
phenotype |
CLINVAR |
Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2).
|
12615169 |
2003 |
|
| Entrez Id: |
4204 |
| Gene Symbol: |
MECP2 |
MECP2
|
0.400 |
CausalMutation
|
phenotype |
CLINVAR |
Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2).
|
12615169 |
2003 |
|
| Entrez Id: |
4204 |
| Gene Symbol: |
MECP2 |
MECP2
|
0.400 |
CausalMutation
|
phenotype |
CLINVAR |
DNA recognition by the methyl-CpG binding domain of MeCP2.
|
11035019 |
2001 |
|
| Entrez Id: |
4204 |
| Gene Symbol: |
MECP2 |
MECP2
|
0.400 |
GeneticVariation
|
phenotype |
CLINVAR |
Epilepsy in a representative series of Rett syndrome.
|
11227330 |
2001 |
|
| Entrez Id: |
4204 |
| Gene Symbol: |
MECP2 |
MECP2
|
0.400 |
CausalMutation
|
phenotype |
CLINVAR |
Epilepsy in a representative series of Rett syndrome.
|
11227330 |
2001 |
|
| Entrez Id: |
4204 |
| Gene Symbol: |
MECP2 |
MECP2
|
0.400 |
GeneticVariation
|
phenotype |
CLINVAR |
DNA recognition by the methyl-CpG binding domain of MeCP2.
|
11035019 |
2001 |
|
| Entrez Id: |
4204 |
| Gene Symbol: |
MECP2 |
MECP2
|
0.400 |
GeneticVariation
|
phenotype |
CLINVAR |
Functional consequences of Rett syndrome mutations on human MeCP2.
|
11058114 |
2000 |
|
| Entrez Id: |
4204 |
| Gene Symbol: |
MECP2 |
MECP2
|
0.400 |
CausalMutation
|
phenotype |
CLINVAR |
Functional consequences of Rett syndrome mutations on human MeCP2.
|
11058114 |
2000 |
|
| Entrez Id: |
4204 |
| Gene Symbol: |
MECP2 |
MECP2
|
0.400 |
GeneticVariation
|
phenotype |
CLINVAR |
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.
|
10508514 |
1999 |
|
| Entrez Id: |
4204 |
| Gene Symbol: |
MECP2 |
MECP2
|
0.400 |
CausalMutation
|
phenotype |
CLINVAR |
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.
|
10508514 |
1999 |
|
| Entrez Id: |
4204 |
| Gene Symbol: |
MECP2 |
MECP2
|
0.400 |
CausalMutation
|
phenotype |
CLINVAR |
Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2.
|
8177735 |
1993 |
|
| Entrez Id: |
4204 |
| Gene Symbol: |
MECP2 |
MECP2
|
0.400 |
GeneticVariation
|
phenotype |
CLINVAR |
Dissection of the methyl-CpG binding domain from the chromosomal protein MeCP2.
|
8177735 |
1993 |