Development and validation of a fetal genotyping assay with potential for noninvasive prenatal diagnosis of hereditary hearing loss. [electronic resource]
Producer: 20170726Description: 1233-1241 p. digitalISSN:- 1097-0223
- Connexin 26 -- genetics
- Connexins -- genetics
- DNA -- blood
- Female
- Genetic Testing -- methods
- Genotype
- Genotyping Techniques -- methods
- Hearing Loss -- congenital
- Heterozygote
- Homozygote
- Humans
- Infant, Newborn
- Membrane Transport Proteins -- genetics
- Mutation
- Phenotype
- Pregnancy
- Prenatal Diagnosis -- methods
- Sulfate Transporters
No physical items for this record
Publication Type: Journal Article; Validation Study
There are no comments on this title.
Log in to your account to post a comment.