No abstract available
MeSH terms
-
Child
-
Chromosome Aberrations / genetics
-
Chromosome Disorders
-
Diagnosis, Differential
-
Female
-
Genes, Dominant / genetics
-
Humans
-
Phenotype
-
Telangiectasia, Hereditary Hemorrhagic / diagnosis
-
Telangiectasia, Hereditary Hemorrhagic / genetics
-
Telangiectasis / diagnosis
-
Telangiectasis / genetics*