Documentos relacionados

1. [PCDH19 gene mutations lead to epilepsy with mental retardation limited to females in 2 cases and literature review].
2. [Long-term results of surgical correction of H-type fistula in girls with a normal anus].
3. Deep phenotyping: symptom annotation made simple with SAMS.
4. [It is normal for classification approaches to be diverse].
5. The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies.
6. Phevor combines multiple biomedical ontologies for accurate identification of disease-causing alleles in single individuals and small nuclear families.
7. [Desquamation of the vascular endothelium after a normal birth and surgical delivery].
8. Genomic Classification of Cutaneous Melanoma.
9. MECP2 variation in Rett syndrome-An overview of current coverage of genetic and phenotype data within existing databases.
10. [Fetal oxygen saturation during normal delivery].