Results: Langer-Giedion Syndrome

Results from Abstracts

Pick one of the followings

*Some genes may be words of complete meaning. In any case, if present, they are relevant key words.

Legend:

***	p-value <= 0.001
**	p-value <= 0.01
*	p-value <= 0.05
n.s.	not significant

Top Ranked Genes, Molecules or Short Names*

Ext1 **
Trps1 *
Pter *
Kcnq3 *
Mb *
She n.s.
Rad21 n.s.
Myc n.s.
Ext2 n.s.
Runx2 n.s.
Th n.s.
Wnt1 n.s.
Sri n.s.
Bmp1 n.s.
Prune n.s.
Anxa13 n.s.
Csmd3 n.s.
Med30 n.s.
Zhx2 n.s.
Zhx1 n.s.
Atad2 n.s.
Derl1 n.s.
Slc30a8 n.s.
Has1 n.s.
Has3 n.s.
Has2 n.s.
Cyp11b2 n.s.
C2 n.s.
Wt1 n.s.
Mbp n.s.
Eif3h n.s.
Gli3 n.s.
Apc n.s.
Mri n.s.
Large n.s.
Set n.s.

Top Ranked Mesh Terms

Chromosome deletion ***
Humans ***
Female ***
Chromosomes human pair 8 ***
Langer-giedion syndrome ***
Genetics ***
Male ***
Adolescent ***
Child **
Child preschool **
Syndrome **
Chromosome banding **
Abnormalities multiple **
Exostoses multiple hereditary **
Karyotyping **
Chromosomes human 6-12 and x **
In situ hybridization fluorescence **
Phenotype *
Diagnostic imaging *
Intellectual disability *
Adult *
Radiography *
Fingers *
Chromosome mapping *
Infant *
Gene deletion *
Seizures *
Nose *
Radius *
Burkitt lymphoma *
Vimentin *
Translocation genetic *
Genomic imprinting *
Sequence deletion *
Facial bones *
Haplotypes *
Transcription factors *
Prenatal diagnosis *
Dna-binding proteins *
Pedigree *
Polymorphism genetic *
Growth substances *
Physical chromosome mapping *
Chromosome aberrations *
Bone morphogenetic proteins *
Cell cycle proteins *
De lange syndrome *
Chondroma *
Tibia *
Ectromelia *
Epiphyses *
Wilms tumor *
Cricetinae *
Prader-willi syndrome *
Nucleic acid hybridization *
Cosmids *
Chromosome disorders *
Psychomotor disorders *
Congenital abnormalities *
N-acetylglucosaminyltransferases *
Chromosome breakage *
Mosaicism *
Comparative genomic hybridization *
Genes dominant *
Mutagenesis insertional *
Fetal death *
Deafness *
Electroencephalography *
Genetic association studies *
Dna primers *
Blotting northern *
Abnormal karyotype *
Genetic linkage *
Bone cysts *
Treatment outcome *
Nuclear proteins *
Dna mutational analysis *
Cytogenetics *
Dna complementary *
Polymerase chain reaction *
Dna *
Polymorphism restriction fragment length *
Chromosomes artificial yeast *
Mutation *
Phosphoproteins *
Cell line *
Pathology *
Base sequence n.s.
Infant newborn n.s.
Lymphocytes n.s.
Classification n.s.
Molecular sequence data n.s.
Diagnosis n.s.
Young adult n.s.
Microcephaly n.s.
Growth disorders n.s.
Middle aged n.s.
Epilepsy n.s.
Genetic markers n.s.
Magnetic resonance imaging n.s.

Results for: Langer-Giedion Syndrome

Results from Abstracts

KEGG Pathways

Gene Ontology Biological Processes