×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
GeneticVariation
disease
CLINVAR
Redefining the MED13L syndrome.
25758992
2015
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
GeneticVariation
disease
CLINVAR
Coupling clinical exome sequencing with functional characterization studies to diagnose a patient with familial Mediterranean fever and MED13L haploinsufficiency syndromes.
28588821
2017
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
GeneticVariation
disease
CLINVAR
MED13L haploinsufficiency syndrome: A de novo frameshift and recurrent intragenic deletions due to parental mosaicism.
28371282
2017
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
GeneticVariation
disease
CLINVAR
MED13L loss-of-function variants in two patients with syndromic Pierre Robin sequence.
29159987
2018
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
GeneticVariation
disease
CLINVAR
Further confirmation of the MED13L haploinsufficiency syndrome.
24781760
2015
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
GeneticVariation
disease
CLINVAR
Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome.
25712080
2015
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
GeneticVariation
disease
CLINVAR
Impaired development of neural-crest cell-derived organs and intellectual disability caused by MED13L haploinsufficiency.
25137640
2014
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
GeneticVariation
disease
CLINVAR
Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing.
25167861
2014
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
GeneticVariation
disease
CLINVAR
De novo mutations in moderate or severe intellectual disability.
25356899
2014
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
GeneticVariation
disease
CLINVAR
Genotype-phenotype evaluation of MED13L defects in the light of a novel truncating and a recurrent missense mutation.
28645799
2017
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
GeneticVariation
disease
CLINVAR
Missense mutations and gene interruption in PROSIT240, a novel TRAP240-like gene, in patients with congenital heart defect (transposition of the great arteries).
14638541
2003
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
GeneticVariation
disease
CLINVAR
UniProt: the universal protein knowledgebase.
27899622
2017
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
GeneticVariation
disease
CLINVAR
[Criteria in the evaluation of blood picture for the diagnosis of bovine leukosis].
5167861
1971
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
GeneticVariation
disease
CLINVAR
Genome sequencing identifies major causes of severe intellectual disability.
24896178
2014
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
GeneticVariation
disease
CLINVAR
Dosage changes of MED13L further delineate its role in congenital heart defects and intellectual disability.
23403903
2013
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
GeneticVariation
disease
CLINVAR
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
24267886
2013
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
CausalMutation
disease
CLINVAR
Redefining the MED13L syndrome.
25758992
2015
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
CausalMutation
disease
CLINVAR
Efficient strategy for the molecular diagnosis of intellectual disability using targeted high-throughput sequencing.
25167861
2014
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
CausalMutation
disease
CLINVAR
Coupling clinical exome sequencing with functional characterization studies to diagnose a patient with familial Mediterranean fever and MED13L haploinsufficiency syndromes.
28588821
2017
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
CausalMutation
disease
CLINVAR
[Criteria in the evaluation of blood picture for the diagnosis of bovine leukosis].
5167861
1971
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
CausalMutation
disease
CLINVAR
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism.
24267886
2013
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
CausalMutation
disease
CLINVAR
Novel de novo heterozygous loss-of-function variants in MED13L and further delineation of the MED13L haploinsufficiency syndrome.
25712080
2015
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
CausalMutation
disease
CLINVAR
MED13L loss-of-function variants in two patients with syndromic Pierre Robin sequence.
29159987
2018
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
CausalMutation
disease
CLINVAR
MED13L haploinsufficiency syndrome: A de novo frameshift and recurrent intragenic deletions due to parental mosaicism.
28371282
2017
×
Entrez Id:
23389
Gene Symbol:
MED13L
MED13L
0.110
CausalMutation
disease
CLINVAR
UniProt: the universal protein knowledgebase.
27899622
2017